FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

API UNISCEPT PLUS AUTOINOCULATOR

K Number: K831341 · Decision Jun 2, 1983
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
65
Applicant Total
57
Review Days
38

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
API UNISCEPT PLUS AUTOINOCULATOR
K Number
K831341
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2500
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Analytical Products, Inc.
Date Received
April 25, 1983
Decision Date
June 2, 1983
Product Code
JTC
Advisory Committee
Microbiology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JTC Device, Microtiter Diluting/Dispensing

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JTC), ordered by most recent decision date.

View all

Other Clearances by Analytical Products, Inc.

K Number Device Name
K924814 API 20E/UNISCEPT 20E
K923684 API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MIC
K922926 API UNISCEPT KB/TYPE 2 AND 3
K901559 MODIFICATION TO API UNISCEPT 20GP
K901390 DMAC INDOLE REAGENT
K895796 API UNISCEPT KB
K884510 MODIFICATION MICRO-MIC
K884509 MODIFICATION MIC/API UNISCEPT(R)
K880598 MODIFICATIONS TO API UNISCEPT (R) KB
K874466 API UNISCEPT(R) MICRO-MIC(R) SYSTEM/UNISCEPT MIC
Search all 57 clearances from Analytical Products, Inc. →