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

SCOTT SELECTICULT-HSV ISOLATION &

K Number: K841680 · Decision Oct 30, 1984
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
36
Applicant Total
16
Review Days
190

Basic Information

Device Name
SCOTT SELECTICULT-HSV ISOLATION &
K Number
K841680
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3305
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
SCOTT LABORATORIES, INC.
Date Received
April 23, 1984
Decision Date
October 30, 1984
Product Code
GQL
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
GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2

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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
K811098 SERO-STAT STAPHYLOCOCCUS TEST
Search all 16 clearances from SCOTT LABORATORIES, INC. →