FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OPUS ESTRADIOL

K Number: K933066 · Decision Sep 8, 1993
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
49
Applicant Total
35
Review Days
78

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Basic Information

Device Name
OPUS ESTRADIOL
K Number
K933066
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1260
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pb Diagnostic Systems, Inc.
Date Received
June 22, 1993
Decision Date
September 8, 1993
Product Code
CHP
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
CHP Radioimmunoassay, Estradiol

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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
K932279 OPUS(R) TOTAL B-HCG TEST SYSTEM
K926131 OPUS MAGNUM ANALYZER
K924957 OPUS(R) VANCOMYCIN
Search all 35 clearances from Pb Diagnostic Systems, Inc. →