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

SERO-STAT STREPTOCOCCUS TEST

K Number: K790492 · Decision May 1, 1979
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
104
Applicant Total
16
Review Days
49

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Basic Information

Device Name
SERO-STAT STREPTOCOCCUS TEST
K Number
K790492
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Scott Laboratories, Inc.
Date Received
March 13, 1979
Decision Date
May 1, 1979
Product Code
GTZ
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
GTZ Antisera, All Groups, Streptococcus Spp.

Similar 510(k) Clearances

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Other Clearances by Scott Laboratories, Inc.

K Number Device Name
K880694 B. CAT CONFIRM
K874933 MUG-INDOLE DISC
K874662 MYCO-FLUOR REAGENT A & B
K873509 IDENTICULT-BL
K871238 ANABAG
K863025 SERO-STAT R II STAPHYLOCOCCUS TEST
K852869 SELECTICULT-CHLAMYDIA
K852832 IDENTICULT-NEISSERIA
K852666 IDENTICULT-AE
K841680 SCOTT SELECTICULT-HSV ISOLATION &
Search all 16 clearances from Scott Laboratories, Inc. →