NEW MODEL STYLES FOR AORTIC ARCH CANNULA
FDA 510(k) clearance K870825 · decided 1987-03-23
Clearance details
- K-number
- K870825
- Device name
- NEW MODEL STYLES FOR AORTIC ARCH CANNULA
- Applicant
- Shiley, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-03-03
- Decision date
- 1987-03-23
- Days to decision
- 20 days
- Clearance type
- Traditional
- Product code
- DQR
- Device class
- 2
- Regulation number
- 870.1300
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Irvine, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| BJORK-SHILEY CARDIAC VALVE (P780008/S013) | Shiley, Inc. | 1986-10-31 |
| BJORK-SHILEY CARDIAC VALVE (P780008/S014) | Shiley, Inc. | 1985-04-09 |
| BJORK-SHILEY CARDIAC VALVE (P780008/S015) | Shiley, Inc. | 1984-11-26 |
| BJORK-SHILEY CARDIAC VALVE (P780008/S011) | Shiley, Inc. | 1984-05-15 |
| BJORK-SHILEY CARDIAC VALVE (P780008/S007) | Shiley, Inc. | 1983-05-20 |
| BJORK-SHILEY CARDIAC VALVE (P780008/S005) | Shiley, Inc. | 1982-02-05 |