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

SELECTICULT-CHLAMYDIA

K Number: K852869 · Decision Sep 19, 1985
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
7
Applicant Total
16
Review Days
73

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Basic Information

Device Name
SELECTICULT-CHLAMYDIA
K Number
K852869
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3120
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Scott Laboratories, Inc.
Date Received
July 8, 1985
Decision Date
September 19, 1985
Product Code
LKH
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
LKH Antisera, Immunoperoxidase, Chlamydia Spp.

Similar 510(k) Clearances

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

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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
K852832 IDENTICULT-NEISSERIA
K852666 IDENTICULT-AE
K841680 SCOTT SELECTICULT-HSV ISOLATION &
K811098 SERO-STAT STAPHYLOCOCCUS TEST
Search all 16 clearances from Scott Laboratories, Inc. →