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

OPUS(R) ROZO

K Number: K911834 · Decision Aug 12, 1991
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
35
Review Days
109

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Basic Information

Device Name
OPUS(R) ROZO
K Number
K911834
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pb Diagnostic Systems, Inc.
Date Received
April 25, 1991
Decision Date
August 12, 1991
Product Code
LGD
Advisory Committee
Microbiology
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
LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

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Other Clearances by Pb Diagnostic Systems, Inc.

K Number Device Name
K940507 OPUS FT4 TEST SYSTEM
K934762 OPUS PROCAINAMIDE TEST SYSTEM
K933389 OPUS CMV-G
K934137 OPUS(R) SEROLOGY CONTROLS, MODIFICATION
K935229 OPUS DIGITOXIN
K934705 OPUS NAPA
K933675 OPUS TOTAL CK
K933066 OPUS ESTRADIOL
K932279 OPUS(R) TOTAL B-HCG TEST SYSTEM
K926131 OPUS MAGNUM ANALYZER
Search all 35 clearances from Pb Diagnostic Systems, Inc. →