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 dna probe, yeast
510(k) Number K931374
FOIA Releasable 510(k) K931374
Device Name AFFIRM VPIII MICROBIAL IDENTIFICATION TEST
Applicant
MICROPROBE CORP.
1725 220TH STREET, S.E., 104
BOTHELL,  WA  98021
Applicant Contact RUSSEL K ENNS
Correspondent
MICROPROBE CORP.
1725 220TH STREET, S.E., 104
BOTHELL,  WA  98021
Correspondent Contact RUSSEL K ENNS
Regulation Number866.2660
Classification Product Code
MLA  
Date Received03/18/1993
Decision Date 06/15/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-