FDA 510(k)
Substantially Equivalent
🇺🇸 United States
COMFEEL PASTE
K Number: K840362
·
Decision Nov 7, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
71
Review Days
286
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Basic Information
- Device Name
- COMFEEL PASTE
- K Number
- K840362
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Coloplast A/S
- Date Received
- January 26, 1984
- Decision Date
- November 7, 1984
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- Third Party
- N
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