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

PANCOAT CORTISOL COATED TUBE RADIOIMMUNOASSAY KIT

K Number: K862336 · Decision Sep 25, 1986
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
83
Applicant Total
16
Review Days
97

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
PANCOAT CORTISOL COATED TUBE RADIOIMMUNOASSAY KIT
K Number
K862336
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1205
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Pantex, Div. Bio-Analysis, Inc.
Date Received
June 20, 1986
Decision Date
September 25, 1986
Product Code
CGR
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
CGR Radioimmunoassay, Cortisol

Similar 510(k) Clearances

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

View all

Other Clearances by Pantex, Div. Bio-Analysis, Inc.

K Number Device Name
K102841 PANTEX AM/PM SALIVARY CORTISOL ENZYME IMMUNOASSAY
K942658 NEOSCREEN ELISA TSH
K914107 PROLACTIN IRMA IMMUNOMAG
K912804 FSH IRMA IMMUNOMAG
K911839 NEONATAL BLOOD SPOT TEST 17-HYDROXPROG RADIO KIT
K911050 LH IRMA IMMUNOMAG
K910717 PANTEX IRMA LH 1251 KIT
K894049 IMMUNOCOAT PROGESTERONE RADIOIMMUNOASSAY KIT
K862483 PANTEX FTE FREE TESTOSTERONE RADIOIMMUNOASSAY KIT
K862447 PANCOAT T3 UPTAKE COATED TUBE RADIOIMMUNOASSAY KIT
Search all 16 clearances from Pantex, Div. Bio-Analysis, Inc. →