• 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 Manual Antimicrobial Susceptibility Test Systems
510(k) Number K864891
Device Name API UNISCEPT (TM) KB
Applicant
Analytical Products, Inc.
200 Express St.
Plainview,  NY  11803
Applicant Contact SUSAN D TIEDY
Correspondent
Analytical Products, Inc.
200 Express St.
Plainview,  NY  11803
Correspondent Contact SUSAN D TIEDY
Regulation Number866.1640
Classification Product Code
JWY  
Date Received12/15/1986
Decision Date 02/20/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-