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

TITERTEK DULUTER/DISPENSER 78-640-00

K Number: K844568 · Decision Jan 30, 1985
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
65
Applicant Total
57
Review Days
68

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Basic Information

Device Name
TITERTEK DULUTER/DISPENSER 78-640-00
K Number
K844568
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2500
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Flow Laboratories, Inc.
Date Received
November 23, 1984
Decision Date
January 30, 1985
Product Code
JTC
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
JTC Device, Microtiter Diluting/Dispensing

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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. →