STRYKER ENCORE STERILIZER
FDA 510(k) clearance K962755 · decided 1997-03-04
Clearance details
- K-number
- K962755
- Device name
- STRYKER ENCORE STERILIZER
- Applicant
- Stryker Corp.
- Decision
- Substantially Equivalent
- Date received
- 1996-07-16
- Decision date
- 1997-03-04
- Days to decision
- 231 days
- Clearance type
- Traditional
- Product code
- FLE
- Device class
- 2
- Regulation number
- 880.6880
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Kalamazoo, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| VITAGEL RT3 SUTGICAL HEMOSTAT (P050044/S033) | Stryker Corp. | 2017-03-02 |
| VITAGEL RT3 SURGICAL HEMOSTAT (P050044/S032) | Stryker Corp. | 2015-07-16 |
| VITAGEL SURGICAL HEMOSTAT (RT3) (P050044/S031) | Stryker Corp. | 2015-04-14 |
| VITAGEL SURGICAL HEMOSTAT (RT3) (P050044/S030) | Stryker Corp. | 2015-04-13 |
| VITAGEL RT3 SURGICAL HEMOSTAT (P050044/S029) | Stryker Corp. | 2014-12-12 |
| VITAGEL RT3 DELIVERY SYSTEM (P050044/S028) | Stryker Corp. | 2014-06-05 |
| VITAGEL SURGICAL HEMOSTAT (VITAGEL) (P050044/S026) | Stryker Corp. | 2014-02-11 |
| RT3 SURGICAL HEMOSTAT (P050044/S027) | Stryker Corp. | 2014-01-27 |