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

UREA/GLUCOSE/CREATININE SERUM RANGE LINEARITY STAN

K Number: K881438 · Decision Jul 6, 1988
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
41
Review Days
92

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Basic Information

Device Name
UREA/GLUCOSE/CREATININE SERUM RANGE LINEARITY STAN
K Number
K881438
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Hichem Diagnostics
Date Received
April 5, 1988
Decision Date
July 6, 1988
Product Code
JJY
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
JJY Multi-Analyte Controls, All Kinds (Assayed)

Similar 510(k) Clearances

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

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Other Clearances by Hichem Diagnostics

K Number Device Name
K981794 HICHEM CALCIUM REAGENT KIT
K963383 HICHEM ALP/AMP REAGENT KIT
K953862 HICHEM ISEKCI SOLUTION KIT 70010
K953860 HICHEM ISE DILUENT KIT 70008
K953861 HICHEM ISE INTDERNAL REFERENCE KIT 70009
K953863 HICHEM ISE STANDARDS KIT 70011
K951751 HICHEM AST REAGENT KIT
K946192 HICHEM Y-GT REAGENT KIT
K946022 HICHEM LDH/L REAGENT KIT
K941433 HI CHEM AQUEOUS GLUCOSE CONTROL, LOW, MED, HIGH
Search all 41 clearances from Hichem Diagnostics →