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

OPUS B12

K Number: K953455 · Decision Aug 23, 1995
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
145
Review Days
35

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Basic Information

Device Name
OPUS B12
K Number
K953455
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1810
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Behring Diagnostics, Inc.
Date Received
July 19, 1995
Decision Date
August 23, 1995
Product Code
CDD
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
CDD Radioassay, Vitamin B12

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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. →