FDA 510(k)
Substantially Equivalent
🇺🇸 United States
GLAUKON
K Number: K812015
·
Decision Feb 8, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
4
Review Days
206
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Basic Information
- Device Name
- GLAUKON
- K Number
- K812015
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Sonometrics Systems, Inc.
- Date Received
- July 17, 1981
- Decision Date
- February 8, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- OP
- Third Party
- N