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

CELL LIFTER

K Number: K871559 · Decision May 15, 1987
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
42
Applicant Total
8
Review Days
23

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Basic Information

Device Name
CELL LIFTER
K Number
K871559
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Corning Costar Corp.
Date Received
April 22, 1987
Decision Date
May 15, 1987
Product Code
LIB
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
LIB Device, General Purpose, Microbiology, Diagnostic

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