FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO ULTIMUM EV HEMOSTASIS INTRODUCER (22F)
K Number: K023447
·
Decision Oct 31, 2002
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
93
Review Days
16
Basic Information
- Device Name
- MODIFICATION TO ULTIMUM EV HEMOSTASIS INTRODUCER (22F)
- K Number
- K023447
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.1340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- ST. JUDE MEDICAL
- Date Received
- October 15, 2002
- Decision Date
- October 31, 2002
- Product Code
- DYB
- 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 |
|---|---|---|---|
| DYB | Introducer, Catheter | FDA class 2 | Cardiovascular |
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