FDA 510(k)
Substantially Equivalent
🇺🇸 United States
DOP 84
K Number: K810155
·
Decision May 1, 1981
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
5
Review Days
100
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Basic Information
- Device Name
- DOP 84
- K Number
- K810155
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Medlog GmbH Marketing Services
- Date Received
- January 21, 1981
- Decision Date
- May 1, 1981
- Advisory Committee
- Unknown
- Review Advisory Committee
- RA
- Third Party
- N