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

IMPROVED THAYER MARTIN MEDIUM

K Number: K760598 · Decision Oct 8, 1976
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
82
Applicant Total
16
Review Days
31

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
IMPROVED THAYER MARTIN MEDIUM
K Number
K760598
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.2410
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Scott Laboratories, Inc.
Date Received
September 7, 1976
Decision Date
October 8, 1976
Product Code
JTY
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
JTY Culture Media, For Isolation Of Pathogenic Neisseria

Similar 510(k) Clearances

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

View all

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. →