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

RIA KIT, PROLACTIN

K Number: K790003 · Decision Mar 12, 1979
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
79
Applicant Total
9
Review Days
69

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
RIA KIT, PROLACTIN
K Number
K790003
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1625
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Cis Radiopharmaceuticals, Inc.
Date Received
January 2, 1979
Decision Date
March 12, 1979
Product Code
CFT
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
CFT Radioimmunoassay, Prolactin (Lactogen)

Similar 510(k) Clearances

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

View all

Other Clearances by Cis Radiopharmaceuticals, Inc.

K Number Device Name
K791860 FERRITIN RIA KIT
K792063 FOLLICLE STIMULATING HORMONE (FSH) KIT
K791202 RIA KIT FOR TRYPSIN
K792000 LUTEINIZING HORMONE (LH) RIA
K791051 PROGESTERONE RADIOIMMUNOASSAY KIT
K780982 KITS, RIA, MYOGLOBIN, HUMAN, MEASUREMENT
K771878 IRIDIUM 192 WIRES & PINS
K760251 SET, ORAL ADMINISTRATION