FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PRO-LOK EXTENSION SET
K Number: K933852
·
Decision Dec 29, 1993
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
4
Review Days
145
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Basic Information
- Device Name
- PRO-LOK EXTENSION SET
- K Number
- K933852
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Beech Medical Products, Inc.
- Date Received
- August 6, 1993
- Decision Date
- December 29, 1993
- Product Code
- FPA
- 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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | FDA class 2 | General Hospital |
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