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

SEPTI-CHEK BH1 BLOOD CULTURE BOTTLE

K Number: K812732 · Decision Oct 19, 1981
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
208
Applicant Total
49
Review Days
21

Basic Information

Device Name
SEPTI-CHEK BH1 BLOOD CULTURE BOTTLE
K Number
K812732
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 19, 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

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