• 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 colorimeter, photometer, spectrophotometer for clinical use
510(k) Number K803285
Device Name PHOTOMETER
Applicant
TURNER DESIGNS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
TURNER DESIGNS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number862.2300
Classification Product Code
JJQ  
Date Received12/30/1980
Decision Date 01/16/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-