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

QUICK-LYTE

K Number: K850209 · Decision Feb 27, 1985
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
161
Applicant Total
20
Review Days
40

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Basic Information

Device Name
QUICK-LYTE
K Number
K850209
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1665
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Seragen Diagnostics, Inc.
Date Received
January 18, 1985
Decision Date
February 27, 1985
Product Code
JGS
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
JGS Electrode, Ion Specific, Sodium

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Other Clearances by Seragen Diagnostics, Inc.

K Number Device Name
K872148 VIVID CHLAMYDIA(TM)
K851663 QUICK-COUNT HEMATOLOGY CONTROLS
K852260 QUICK-CHEM CALIBRATION SET
K851520 CK/LD ISOENZYMES CONTROLS(HUMAN)
K851521 LD-1(IMMUNO) SEPARATION SET
K844743 SERATEST ENA(RNP/SM) DETERMINATION
K842563 SERATEST DNA DETERMINATION
K841504 QUICK-COUNT PLUS 2
K840793 CK/MB IMMUNO-ISOENZYME CONTROL SERUM
K840863 SERATEST RF LATEX DETERMINATION
Search all 20 clearances from Seragen Diagnostics, Inc. →