PERMANENT PACING LEAD, MODEL PY2
FDA 510(k) clearance K041809 · decided 2004-08-06
Clearance details
- K-number
- K041809
- Device name
- PERMANENT PACING LEAD, MODEL PY2
- Applicant
- Oscor, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2004-07-06
- Decision date
- 2004-08-06
- Days to decision
- 31 days
- Clearance type
- Special
- Product code
- DTB
- Device class
- 3
- Regulation number
- 870.3680
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Palm Harbor, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Permanent Pacing Lead (Catalog #: 03332, 03334, 03337, 03107, 03116, 03108, 03109, 05756, recall (Z-2333-2008) | Oscor, Inc. | 2008-09-24 |