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

LIQUISOL PROGESTERONE RADIOIMMUNO

K Number: K820686 · Decision Apr 1, 1982
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
56
Applicant Total
11
Review Days
21

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Basic Information

Device Name
LIQUISOL PROGESTERONE RADIOIMMUNO
K Number
K820686
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1620
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Damon Corp.
Date Received
March 11, 1982
Decision Date
April 1, 1982
Product Code
JLS
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
JLS Radioimmunoassay, Progesterone

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Other Clearances by Damon Corp.

K Number Device Name
K874865 DAMON D.E.T.E.C.T IMAGE ENHANCER
K831826 ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY
K802661 LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT
K790250 LIQUISOL CORTISOL RIA TEST KIT
K782124 IEC CENTRA-7 CENTRIFUGE MODEL 2362
K781012 RIA TEST KIT SYS. DAMON KIQUISOL FREE
K780207 LIQUISOL DIGOXIN RIA TEST KIT
K770918 LIQUI SOL T4 RIA TEST KIT
K770606 ANALYZEO, PLASMA, BLOOD, COLYSAGRAPH
K761013 SPINETTE CENTRIFUGE
Search all 11 clearances from Damon Corp. →