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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