SCHNEIDER SIDEKICK MONORAIL Y-CONNECTOR
FDA 510(k) clearance K897082 · decided 1990-03-06
Clearance details
- K-number
- K897082
- Device name
- SCHNEIDER SIDEKICK MONORAIL Y-CONNECTOR
- Applicant
- Schneider Intl., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1989-12-20
- Decision date
- 1990-03-06
- Days to decision
- 76 days
- Clearance type
- Traditional
- Product code
- DQY
- Device class
- 2
- Regulation number
- 870.1250
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Minneapolis, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.