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

SAS(TM) SERUM/URINE HCG

K Number: K932409 · Decision Jun 29, 1993
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
71
Applicant Total
199
Review Days
42

Basic Information

Device Name
SAS(TM) SERUM/URINE HCG
K Number
K932409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SA SCIENTIFIC, INC.
Date Received
May 18, 1993
Decision Date
June 29, 1993
Product Code
DHA
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
DHA System, Test, Human Chorionic Gonadotropin

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K100227 SAS FLUALERT A&B, SAS INFLUENZA A TEST
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K041439 SAS INFLUENZA B TEST
K041441 SAS INFLUENZA A TEST
K030628 SAS RSV CONTROL KIT
K022845 SAS RSV TEST
K022683 SAS BLOOD/SERUM/URINE/URINE HCG
K023270 SAS STREPALERT
K020438 SAS VALUE HCG
K013379 SAS STREPALERT
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