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

MICROMEDIC REAGENT DISPENSER

K Number: K803252 · Decision Jan 12, 1981
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
65
Applicant Total
42
Review Days
20

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Basic Information

Device Name
MICROMEDIC REAGENT DISPENSER
K Number
K803252
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2500
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Micromedic Systems
Date Received
December 23, 1980
Decision Date
January 12, 1981
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 Micromedic Systems

K Number Device Name
K923643 MEDICOOL
K872309 MICROMEDIC COMBOSTAT LH/FSH KIT
K871505 AUTOPAK NEONATAL TSH MONOCLONAL IRMA KIT
K871008 MICROMEDIC NEONATAL T4 KIT
K870904 MICROMEDIC NEONATAL TSH MONOCLONAL IRMA KIT
K870245 AUTOPAK TSH MONOCLONAL IRMA KIT
K862206 TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER
K860813 MICROMEDIC HTSH MONOCLONAL IRMA KIT
K861262 MMS T3 UPTAKE
K861320 MMS T4 RIA KIT
Search all 42 clearances from Micromedic Systems →