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

ELISA RUBELLA IGM

K Number: K914420 · Decision Dec 27, 1991
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
82
Review Days
85

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Basic Information

Device Name
ELISA RUBELLA IGM
K Number
K914420
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sclavo, Inc.
Date Received
October 3, 1991
Decision Date
December 27, 1991
Product Code
LFX
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
LFX Enzyme Linked Immunoabsorbent Assay, Rubella

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Other Clearances by Sclavo, Inc.

K Number Device Name
K914789 ELISA CMV IGM
K914852 ELISA TOXO IGM
K895943 NORMAL AND ABNORMAL CONTROL SERA
K895822 TOTAL BILIRUBIN L.F.
K895847 CREATININE 340 (ENZYMATIC)
K880049 CHOLINESTERASE - BUTYRYTHIOCHOLINE SUBSTRATE
K880199 CHOLINESTERASE - ACETYTHIOCHOLINE SUBSTRATE
K873496 ATYPICAL CHOLINESTERASE
K884035 SAITRON 430 RANDOM ACCESS CHEMISTRY ANALYZER
K884649 TOTAL IRON BINDING CAPACITY TEST
Search all 82 clearances from Sclavo, Inc. →