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

OPUS(R) TOBRAMYCIN

K Number: K911940 · Decision Jul 1, 1991
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
16
Applicant Total
35
Review Days
61

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Basic Information

Device Name
OPUS(R) TOBRAMYCIN
K Number
K911940
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3900
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pb Diagnostic Systems, Inc.
Date Received
May 1, 1991
Decision Date
July 1, 1991
Product Code
LCR
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
LCR Fluorescent Immunoassay, Tobramycin

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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. →