FDA PMA FDA Class 2 Approved 🇺🇸 United States

Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

PMA: P850048 · Supplement: S011 · Decision Nov 6, 1995
Classifications
1
FEI Numbers
37
Registration Numbers
37

Basic Information

Device Name
Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers
Trade Name
TANDEM-R PSA IMMUNORADIOMETRIC ASSAY IMMUNOMETRIC TANDEM-E PSA IMMUNORADIOMETRIC ASSAY
PMA Number
P850048
Supplement Number
S011
Device Class
FDA Class 2
Product Code
LTJ
Generic Name
PROSTATE-SPECIFIC ANTIGEN (PSA) FOR MANAGEMENT OF PROSTATE CANCERS
Regulation Number
866.6010
Medical Specialty
Immunology
Advisory Committee
Immunology
Decision
Approved
Decision Code
APPR
Decision Date
November 6, 1995
Date Received
June 14, 1995
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR INCLUSION OF INFORMATION AND ATA ON PSA FORMS IN THE TANDEM PSA LABELING

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LTJ Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers