FDA 510(k) Substantially Equivalent 🇺🇸 United States

LASERSPEC

K Number: K841430 · Decision Dec 13, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
10
Review Days
251

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Basic Information

Device Name
LASERSPEC
K Number
K841430
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Clement Clarke, Inc.
Date Received
April 6, 1984
Decision Date
December 13, 1984
Advisory Committee
Unknown
Review Advisory Committee
OP
Third Party
N

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