FDA 510(k)
Substantially Equivalent
🇺🇸 United States
P105
K Number: K820827
·
Decision Jun 25, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
4
Review Days
91
Basic Information
- Device Name
- P105
- K Number
- K820827
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- EUROTAN INTL.
- Date Received
- March 26, 1982
- Decision Date
- June 25, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- PM
- Third Party
- N