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

MICROMEDIC AUTOMATIC DILUTER

K Number: K800606 · Decision Apr 16, 1980
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
139
Applicant Total
42
Review Days
30

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Basic Information

Device Name
MICROMEDIC AUTOMATIC DILUTER
K Number
K800606
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2750
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Micromedic Systems
Date Received
March 17, 1980
Decision Date
April 16, 1980
Product Code
JQW
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
JQW Station, Pipetting And Diluting, For Clinical Use

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
K860813 MICROMEDIC HTSH MONOCLONAL IRMA KIT
K861262 MMS T3 UPTAKE
K861320 MMS T4 RIA KIT
Search all 42 clearances from Micromedic Systems →