FDA 510(k) Substantially Equivalent 🇺🇸 United States

DIAGNOSTIC MICROSOPCE SLIDES

K Number: K844092 · Decision Oct 25, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
37
Review Days
6

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Basic Information

Device Name
DIAGNOSTIC MICROSOPCE SLIDES
K Number
K844092
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Sybron Corp.
Date Received
October 19, 1984
Decision Date
October 25, 1984
Advisory Committee
Unknown
Review Advisory Committee
CH
Third Party
N

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