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

OPUS PSA TEST SYSTEM

K Number: K964595 · Decision Jun 24, 1997
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
33
Applicant Total
145
Review Days
218

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
OPUS PSA TEST SYSTEM
K Number
K964595
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.6010
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Behring Diagnostics, Inc.
Date Received
November 18, 1996
Decision Date
June 24, 1997
Product Code
LTJ
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) 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

Similar 510(k) Clearances

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

View all

Other Clearances by Behring Diagnostics, Inc.

K Number Device Name
K973832 OPUS HLH CONTROLS
K972929 N ANTISERUM TO HUMAN ALBUMIN
K972840 N ANTISERUM TO HUMAN TRANSFERRIN
K973202 MODIFICATION OF OPUS FERRITIN TEST SYSTEM
K972316 OPUS D-DIMER
K972116 VON WILLEBRAND REAGENT
K972011 OPUS ETHANOL
K971600 EMIT CALIBRATOR B LEVEL 1 (CUTOFF)/EMIT CALIBRATOR B LEVEL 2 (HIGH)
K971596 EMIT II OPIATES 300/2000 ASSAY
K971725 OPUS PROGESTERONE
Search all 145 clearances from Behring Diagnostics, Inc. →