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

MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)

K Number: K853127 · Decision Sep 16, 1985
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
42
Review Days
53

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)
K Number
K853127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1810
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Micromedic Systems
Date Received
July 25, 1985
Decision Date
September 16, 1985
Product Code
CDD
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
CDD Radioassay, Vitamin B12

Similar 510(k) Clearances

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

View all

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 →