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

SERAGAN ACTH125 I-RIA KIT

K Number: K822115 · Decision Oct 18, 1982
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
29
Applicant Total
20
Review Days
91

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Basic Information

Device Name
SERAGAN ACTH125 I-RIA KIT
K Number
K822115
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1025
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Seragen Diagnostics, Inc.
Date Received
July 19, 1982
Decision Date
October 18, 1982
Product Code
CKG
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
CKG Radioimmunoassay, Acth

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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
K850209 QUICK-LYTE
K844743 SERATEST ENA(RNP/SM) DETERMINATION
K842563 SERATEST DNA DETERMINATION
K841504 QUICK-COUNT PLUS 2
K840793 CK/MB IMMUNO-ISOENZYME CONTROL SERUM
Search all 20 clearances from Seragen Diagnostics, Inc. →