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

TITERTEK MICROPLATE INCUBATOR

K Number: K812340 · Decision Sep 23, 1981
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
11
Applicant Total
57
Review Days
36

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
TITERTEK MICROPLATE INCUBATOR
K Number
K812340
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2540
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Flow Laboratories, Inc.
Date Received
August 18, 1981
Decision Date
September 23, 1981
Product Code
JTQ
Advisory Committee
Microbiology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JTQ Bath, Incubators/Water, All

Similar 510(k) Clearances

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

View all

Other Clearances by Flow Laboratories, Inc.

K Number Device Name
K861897 UNISKAN II
K862066 TITERTEK MICROPLATE WASHER S-12
K861823 GENTAMICIN SULFATE SOLUTION (50MG GENTAMICIN)
K861824 GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)
K861791 PENICILLIN-STREPTOMYCIN-FUNGIZONE
K860752 GOAT SERUM (29-391-54)
K860762 GAMMA-FREE HORSE SERUM
K850908 TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA
K844418 TITERTEK MULTISKAN MCC
K844419 TITERTEK MULTISKAN MSS/340
Search all 57 clearances from Flow Laboratories, Inc. →