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

DIFFERENTIAL MEDIA

K Number: K873262 · Decision Oct 28, 1987
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
284
Applicant Total
14
Review Days
78

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Basic Information

Device Name
DIFFERENTIAL MEDIA
K Number
K873262
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2360
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Central Media
Date Received
August 11, 1987
Decision Date
October 28, 1987
Product Code
JSI
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
JSI Culture Media, Selective And Differential

Similar 510(k) Clearances

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

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Other Clearances by Central Media

K Number Device Name
K873259 SPECIALTY MEDIA
K873257 GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.
K873258 STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIA
K873260 CORYNEBACTERIA ISOLATION MEDIA
K873267 ECG BASED MEDIA
K873270 ACTINOMYCETE DIFFERENTIAL MEDIA
K873268 MUELLER HINTON MEDIA
K873269 MYCOLOGICAL MEDIA
K873266 MIDDLEBROOK BASED MEDIA
K873265 MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION
Search all 14 clearances from Central Media →