FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

IMMUNO/FEBRILE ANTIGENS

K Number: K883685 · Decision Sep 28, 1988
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
59
Applicant Total
11
Review Days
30

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Basic Information

Device Name
IMMUNO/FEBRILE ANTIGENS
K Number
K883685
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3550
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Immunostics Co., Inc.
Date Received
August 29, 1988
Decision Date
September 28, 1988
Product Code
GNC
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
GNC Antigens, Febrile, Slide And Tube, All Groups, Salmonella Spp.

Similar 510(k) Clearances

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

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Other Clearances by Immunostics Co., Inc.

K Number Device Name
K926569 IMMUNO RA UNDILUTED
K902360 HEMA-SCREEN
K894780 IMMUNO/ASO
K872910 IMMUNO/SLE
K863741 IMMUNO-CEPT D (BETA-MONOCLONAL)
K854619 DETECTACULT
K853105 IMMUNO-IM
K842110 SLIDE PREGNANCY TEST
K834390 IMMUNO-CRP
K834391 IMMUNO-RA
Search all 11 clearances from Immunostics Co., Inc. →