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

IMX FOLATE

K Number: K943691 · Decision Mar 23, 1995
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
63
Applicant Total
14
Review Days
237

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Basic Information

Device Name
IMX FOLATE
K Number
K943691
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1295
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Mfg., Inc.
Date Received
July 29, 1994
Decision Date
March 23, 1995
Product Code
CGN
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
CGN Acid, Folic, Radioimmunoassay

Similar 510(k) Clearances

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Other Clearances by Abbott Mfg., Inc.

K Number Device Name
K981457 ALBP
K981232 CA
K981231 CO2
K965230 ABBOTT LIFECARE STANDARD TUBING INFUSION PUMP
K971293 LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVE
K953656 ABBOTT IMX PROLACTIN(MODIFICATION)
K953657 ABBOTT AXSYM PROLACTIN(MODIFICATION)
K944669 FLEXIFLO QUANTUM ENTERAL PUMP
K943733 FLEXIFLO SIX ENTERAL NUTRITION PUMP
K941214 LIFESHIELD EXTENSION SET
Search all 14 clearances from Abbott Mfg., Inc. →