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

DIASCAN AQUEOUS GLUCOSE CONTROL LOW, DIASCAN AQUEOUS GLUCOSE CONTROL HIGH

K Number: K973677 · Decision Dec 15, 1997
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
3
Review Days
80

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Basic Information

Device Name
DIASCAN AQUEOUS GLUCOSE CONTROL LOW, DIASCAN AQUEOUS GLUCOSE CONTROL HIGH
K Number
K973677
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sorrento Biochemical, Inc.
Date Received
September 26, 1997
Decision Date
December 15, 1997
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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

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Other Clearances by Sorrento Biochemical, Inc.

K Number Device Name
K973676 PRESTIGE AQUEOUS GLUCOSE CONTROL LOW, PRESTIGE AQUEOUS GLUCOSE CONTROL HIGH
K973678 ULTRA + AQUEOUS GLUCLOSE CONTROL LOW ULTRA + AQUEOUS GLUCOSE CONTROL HIGH