FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GENERAL PROCEDURE KIT
K Number: K960248
·
Decision Apr 12, 1996
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
4
Review Days
87
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Basic Information
- Device Name
- GENERAL PROCEDURE KIT
- K Number
- K960248
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5860
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Physician Industries, Inc.
- Date Received
- January 16, 1996
- Decision Date
- April 12, 1996
- Product Code
- FMF
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FMF | Syringe, Piston | FDA class 2 | General Hospital |
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