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

SEPTI-CHEK COLUMBIA BROTH BLOOD CULTURE

K Number: K812730 · Decision Oct 23, 1981
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
208
Applicant Total
49
Review Days
25

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
SEPTI-CHEK COLUMBIA BROTH BLOOD CULTURE
K Number
K812730
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2300
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Hoffmann-La Roche, Inc.
Date Received
September 28, 1981
Decision Date
October 23, 1981
Product Code
JSG
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
JSG Culture Media, Non-Selective And Non-Differential

Similar 510(k) Clearances

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

View all

Other Clearances by Hoffmann-La Roche, Inc.

K Number Device Name
K850727 BHCG-ROCHE EIA
K831694 RENAK
K830481 ABUSCREEN RADIOIMMUNOASSAY-PHENCYCLIDINE
K830480 ABUSCREEN RADIOIMMUNOASSAY-COCAINE META
K830461 ABUSCREEN RADIOUMMUNOASSAY-METHAQUALONE
K830460 ABUSCREEN RADIOIMMUNOASSAY FOR MORPHINE
K830482 ABUSCREEN RADIOIMMUNOASSAY-AMPHETAMINE
K830462 ABUSCREEN RADIOUMMUNOASSAY--URINE
K830479 ABUSCREEN RADIOIMMUNOASSAY-BARBITURATE
K823579 COBAS REAGENT FOR TOTAL PROTEIN
Search all 49 clearances from Hoffmann-La Roche, Inc. →