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 sponge, ophthalmic
510(k) Number K842990
Device Name STERILE EYE SURGERY KITS
Applicant
BIOLOGICAL & ENVIRONMENTAL CONTROL LABORATORIES
615 FRONT ST.
TOLEDO,  OH  43605
Applicant Contact JAMES P KULLA
Correspondent
BIOLOGICAL & ENVIRONMENTAL CONTROL LABORATORIES
615 FRONT ST.
TOLEDO,  OH  43605
Correspondent Contact JAMES P KULLA
Regulation Number886.4790
Classification Product Code
HOZ  
Date Received07/30/1984
Decision Date 05/09/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-