Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

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


New Search Back To Search Results
Device Classification Name instrument, vitreous aspiration and cutting, ac-powered
510(k) Number K940746
Device Name VIT CUTTER MODEL 94
Applicant
VISION CARE DEVICES, INC.
1246 REDWOOD BLVD.
REDDING,  CA  96003
Applicant Contact CHET CRACCHIOLO
Correspondent
VISION CARE DEVICES, INC.
1246 REDWOOD BLVD.
REDDING,  CA  96003
Correspondent Contact CHET CRACCHIOLO
Regulation Number886.4150
Classification Product Code
HQE  
Date Received02/18/1994
Decision Date 06/06/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-