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

CLINALYZER MODEL VX-1000

K Number: K851638 · Decision May 13, 1985
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
207
Applicant Total
33
Review Days
24

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Basic Information

Device Name
CLINALYZER MODEL VX-1000
K Number
K851638
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Alpkem Corp.
Date Received
April 19, 1985
Decision Date
May 13, 1985
Product Code
JJE
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
JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

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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
K890332 RFA/2 RAPID FLOW ANALYZER W/COMPUTER
K890335 SODIUM HYDROXIDE SOLUTION, CREATININE REAG./DILU.
K890333 ALBUMIN REAGENT
K883020 RFA-300 RAPID FLOW ANALYZER W/COMPUTER
K860367 MAGNESIUM (SUBSTRATE, ENZYME, REAGENT)
Search all 33 clearances from Alpkem Corp. →