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

LA-STAPH IDENTIFICATION SYSTEM

K Number: K831918 · Decision Jun 8, 1983
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
19
Applicant Total
26
Review Days

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
LA-STAPH IDENTIFICATION SYSTEM
K Number
K831918
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Immuno-Mycologics, Inc.
Date Received
June 8, 1983
Decision Date
June 8, 1983
Product Code
JWX
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
JWX Kit, Screening, Staphylococcus Aureus

Similar 510(k) Clearances

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

View all

Other Clearances by Immuno-Mycologics, Inc.

K Number Device Name
K120946 ALPHA CRYPTOCOCCAL ANTIGEN EIA
K112422 CRAG LATERAL FLOW ASSAY (LFA)
K102286 CRAG LATERAL FLOW ASSAY (CRAG LFA)
K101407 ALPHA HISTOPLASMA ANTIGEN EIA MODEL HAG102
K883333 RABBIT PLASMA FIBRINOGEN (RPF) SUPPLEMENT
K880029 EXO-ANTIGEN IDENTIFICATION SYSTEM CAT.# EX1001
K843286 EI-CANDIDA ENZYME IMMUNOASSAY EI1001
K830837 LA-HISTO ANTIBODY SYSTEM #HL 1001
K810510 YA-CRYPTO ANTIBODY TUBE AGGLUTINATION
K802427 LA-SPORO ANTIBODY SYSTEM
Search all 26 clearances from Immuno-Mycologics, Inc. →