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

ENZYGNOST TOXOPLASMOSIS/IGM

K Number: K913505 · Decision Mar 4, 1992
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
105
Applicant Total
145
Review Days
210

Basic Information

Device Name
ENZYGNOST TOXOPLASMOSIS/IGM
K Number
K913505
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BEHRING DIAGNOSTICS, INC.
Date Received
August 7, 1991
Decision Date
March 4, 1992
Product Code
LGD
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LGD), 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
K964595 OPUS PSA TEST SYSTEM
Search all 145 clearances from BEHRING DIAGNOSTICS, INC. →