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

LUTEINIZING HORMONE (LH-IRMA) RIA KIT

K Number: K864144 · Decision Nov 24, 1986
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
18
Review Days
33

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
LUTEINIZING HORMONE (LH-IRMA) RIA KIT
K Number
K864144
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Immuchem Corp.
Date Received
October 22, 1986
Decision Date
November 24, 1986
Product Code
CEP
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
CEP Radioimmunoassay, Luteinizing Hormone

Similar 510(k) Clearances

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

View all

Other Clearances by Immuchem Corp.

K Number Device Name
K883726 THYROID STIMULATING HORMONE (HTSH) IRMA NEONATAL
K871317 FOLLICLE STIMULATING HORMONE (HFSH)
K871542 HPROLACTIN KIT
K865071 THYROID STIMULATING HORMONE (TSH IRMA) RIA KIT
K860559 ANDROSTENEDIONE 125I KIT BY RIA
K854094 IMMUCHEM COVALENT COAT A SOLID PHASE RADIOIMMUNOAS
K830962 IMMUCHEM COVALENT-COAT RIA KIT
K822509 COVALENT COAT RIA KIT
K822140 IMMUCHEM COVALENT-COAT
K820329 ESTRADIOL KIT BY RIA
Search all 18 clearances from Immuchem Corp. →