• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards | Inspections
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameBOSTON EQUEALENS RIGID GAS/II RIGID GAS PERMEABLE CONTACT LENS
Classification Namelens,contact(rigid gas permeable)-extended wear
Generic Namerigid gas permeable contact lens
Regulation Number886.5916
ApplicantBAUSCH & LOMB, INC.
PMA NumberP860022
Supplement NumberS054
Date Received01/30/2002
Decision Date05/06/2002
Product Code
MWL[ Registered Establishments with MWL ]
Advisory Committee Ophthalmic
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - specifications
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for an aspheric design for extended wear and labeling changes for the device. Requested labeling changes include: 1) change from the title "patient instructions" to "patient care guide". 2) update the prescription caution statement. 3) modify the product description section of the package insert and professional fitting and information guide as follows: a) add the descriptions for both the aspheric design (extended and daily wear) and the previously approved bifocal lens (daily wear only) and specify daily wear for the toric and bifocal designs; b) remove from these product description sections the phrase "without uv" because this option is no longer available; and c) change the color name of the blue lens material from "dark blue" to "electric blue". 4) correct the manufacturer's address. 5) update the wording of the uv warning and clarify the extended wear indication as in the indication stated below. "the boston equalens (itafluorofocon a) rgp contact lens is indicated for daily or extended wear from 1 to 7 days between removals for cleaning and disinfection as recommended by the eye care practitioner. The lens is indicated for extended wear for the correction of refractive ametropia (myopia and hyperopia) in not-aphakic persons with non-diseased eyes in powers from -20. 00d to +12. 00d. The lens is indicated for daily wear for the correction of refractive ametropia (myopia, hyperopia, astigmatism and presbyopia) in aphakic and not-aphakic persons with non-diseased eyes. The lens may be disinfected using a chemical disinfection system only. ".
-
-