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

RFA/2 RAPID FLOW ANALYZER W/COMPUTER

K Number: K890332 · Decision Feb 17, 1989
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
31
Applicant Total
33
Review Days
25

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Basic Information

Device Name
RFA/2 RAPID FLOW ANALYZER W/COMPUTER
K Number
K890332
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Alpkem Corp.
Date Received
January 23, 1989
Decision Date
February 17, 1989
Product Code
JJC
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
JJC Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use

Similar 510(k) Clearances

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

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Other Clearances by Alpkem Corp.

K Number Device Name
K894011 TOTAL GALACTOSE
K891070 PHENYLALANINE (NINHYDRIN REACTION)
K890334 TOTAL CHOLESTEROL REAGENT
K890337 TRIGLYCERIDES - GPO REAGENT
K890336 GLUCOSE (GOD) REAGENT
K890335 SODIUM HYDROXIDE SOLUTION, CREATININE REAG./DILU.
K890333 ALBUMIN REAGENT
K883020 RFA-300 RAPID FLOW ANALYZER W/COMPUTER
K860367 MAGNESIUM (SUBSTRATE, ENZYME, REAGENT)
K851990 INTERNAL STANDARD SOLUTION, EXTERNAL STANDARD SOLU
Search all 33 clearances from Alpkem Corp. →