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 tape, measuring, rulers and calipers
510(k) Number K932112
Device Name OLYMPIC INFA-LENGTH
Applicant
OLYMPIC MEDICAL CORP.
5900 FIRST AVE., SOUTH
SEATTLE,  WA  98108
Applicant Contact JOSEPH STEFANILE
Correspondent
OLYMPIC MEDICAL CORP.
5900 FIRST AVE., SOUTH
SEATTLE,  WA  98108
Correspondent Contact JOSEPH STEFANILE
Regulation Number878.4800
Classification Product Code
FTY  
Date Received05/03/1993
Decision Date 07/22/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-