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

DIFFERENTIAL CULTURE MEDIUM

K Number: K850734 · Decision Mar 20, 1985
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
52
Applicant Total
8
Review Days
28

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Basic Information

Device Name
DIFFERENTIAL CULTURE MEDIUM
K Number
K850734
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2320
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Roseville Medical Laboratoriesu
Date Received
February 20, 1985
Decision Date
March 20, 1985
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 Roseville Medical Laboratoriesu

K Number Device Name
K850731 CULTURE MEDIUM FOR ANTIMICROBIAL SUSCEP. TESTING
K850738 SUPPLEMENT FOR CULTURE MEDIUM
K850737 TRANSPORT CULTURE MEDIUM
K850736 SELECTIVE CULTURE MEDIUM
K850733 MULTIPURPOSE CULTURE MEDIUM
K850732 CULTURE MEDIUM FOR PATHOGENIC NEISSERIA SSP.MI
K850735 ENRICHED CULTURE MEDIUM