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

I-ESTRIOL TEST SET

K Number: K781599 · Decision Oct 17, 1978
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
41
Applicant Total
13
Review Days
29

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
I-ESTRIOL TEST SET
K Number
K781599
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1265
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Wien Laboratories, Inc.
Date Received
September 18, 1978
Decision Date
October 17, 1978
Product Code
CGI
Advisory Committee
Clinical Chemistry
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CGI Radioimmunoassay, Estriol

Similar 510(k) Clearances

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

View all

Other Clearances by Wien Laboratories, Inc.

K Number Device Name
K912850 SHBG
K834246 PROGESTERONE TEST SET 125I 17-OH
K832452 ANDROSTENEDIONE TEST SET 125I
K823200 125 I-DEHYDROEPIANDROSTERONE SULFATE
K821653 PROTRIPTYLINE TRI-CY TEST SET
K821652 DOXEPIN TRI-CY TEST SET
K802728 125I-TESTOSTERONE TEST SET
K792041 DHEA-SULFATE TEST SET
K781834 TEST SET, 125 I-DIGOXIN
K772306 125I DIGOXIN TEST SET
Search all 13 clearances from Wien Laboratories, Inc. →