MODIFIED DECANNULATION STOPPER
FDA 510(k) clearance K894050 · decided 1989-08-01
Clearance details
- K-number
- K894050
- Device name
- MODIFIED DECANNULATION STOPPER
- Applicant
- Premier Medical
- Decision
- Substantially Equivalent
- Date received
- 1989-06-07
- Decision date
- 1989-08-01
- Days to decision
- 55 days
- Clearance type
- Traditional
- Product code
- JOH
- Device class
- 2
- Regulation number
- 868.5800
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Philadelphia, PA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.