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

INSULIN AUTOPAK

K Number: K781086 · Decision Aug 14, 1978
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
26
Applicant Total
42
Review Days
46

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Basic Information

Device Name
INSULIN AUTOPAK
K Number
K781086
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1405
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Micromedic Systems
Date Received
June 29, 1978
Decision Date
August 14, 1978
Product Code
CFP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
CFP Radioimmunoassay, Immunoreactive Insulin

Similar 510(k) Clearances

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

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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 →