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

TITERTEK MULTISKAN MCC

K Number: K844418 · Decision Mar 21, 1985
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
57
Review Days
126

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Basic Information

Device Name
TITERTEK MULTISKAN MCC
K Number
K844418
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Flow Laboratories, Inc.
Date Received
November 15, 1984
Decision Date
March 21, 1985
Product Code
JJQ
Advisory Committee
Clinical Chemistry
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
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

Similar 510(k) Clearances

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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
K844419 TITERTEK MULTISKAN MSS/340
K844567 TITERTEK TWINREADER 78-630-00
Search all 57 clearances from Flow Laboratories, Inc. →