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

VISTA ANTIGEN SALMONELLA H D

K Number: K972389 · Decision Aug 25, 1997
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
59
Applicant Total
10
Review Days
60

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Basic Information

Device Name
VISTA ANTIGEN SALMONELLA H D
K Number
K972389
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3550
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lee Laboratories, Inc.
Date Received
June 26, 1997
Decision Date
August 25, 1997
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.

View all

Other Clearances by Lee Laboratories, Inc.

K Number Device Name
K972392 VISTA ANTIGEN SALMONELLA H A
K972391 VISTA ANTIGEN SALMONELLA H B
K972386 VISTA ANTIGEN SALMONELLA O GROUP B
K972396 VISTA ANTIGEN BRUCELLA MELITENSIS
K972395 VISTA ANTIGEN SALMONELLA O GROUP D
K972390 VISTA ANTIGEN SALMONELLA H C
K972388 VISTA ANTIGEN SALMONELLA O GROUP C
K972387 VISTA ANTIGEN SALMONELLA O GROUP A
K972394 VISTA ANTIGEN BRUCELLA ABORTUS