FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MULLINS-X, MODEL 250X
K Number: K082868
·
Decision Oct 24, 2008
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
44
Review Days
25
Basic Information
- Device Name
- MULLINS-X, MODEL 250X
- K Number
- K082868
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.1250
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- NUMED, INC.
- Date Received
- September 29, 2008
- Decision Date
- October 24, 2008
- Product Code
- DQY
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DQY | Catheter, Percutaneous | FDA class 2 | Cardiovascular |
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