FDA 510(k)
FDA class 1
Unknown
🇺🇸 United States
PRIA-KIT (TM) PRIAPISM KIT S.S.
K Number: K874000
·
Decision Dec 30, 1987
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
1
Review Days
90
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Basic Information
- Device Name
- PRIA-KIT (TM) PRIAPISM KIT S.S.
- K Number
- K874000
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Unknown
- Applicant
- Canton Medical, Inc.
- Date Received
- October 1, 1987
- Decision Date
- December 30, 1987
- Product Code
- GAA
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- GU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GAA | Needle, Aspiration And Injection, Disposable | FDA class 1 | General, Plastic Surgery |
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