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

API 3S

K Number: K770176 · Decision Feb 18, 1977
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
52
Applicant Total
57
Review Days
23

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Basic Information

Device Name
API 3S
K Number
K770176
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2320
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Analytical Products, Inc.
Date Received
January 26, 1977
Decision Date
February 18, 1977
Product Code
JSE
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
JSE Culture Media, Multiple Biochemical Test

Similar 510(k) Clearances

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

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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. →