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

MICROMEDIC HTSH MONOCLONAL IRMA KIT

K Number: K860813 · Decision Jul 14, 1986
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
42
Review Days
132

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Basic Information

Device Name
MICROMEDIC HTSH MONOCLONAL IRMA KIT
K Number
K860813
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Micromedic Systems
Date Received
March 4, 1986
Decision Date
July 14, 1986
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

Similar 510(k) Clearances

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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
K861262 MMS T3 UPTAKE
K861320 MMS T4 RIA KIT
K853127 MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)
Search all 42 clearances from Micromedic Systems →