VALVE, VENT-AWAY TWO-WAY
FDA 510(k) clearance K781920 · decided 1978-12-04
Clearance details
- K-number
- K781920
- Device name
- VALVE, VENT-AWAY TWO-WAY
- Applicant
- Chesebrough-Pond'S U.S.A. Co.
- Decision
- Substantially Equivalent
- Date received
- 1978-11-13
- Decision date
- 1978-12-04
- Days to decision
- 21 days
- Clearance type
- Traditional
- Product code
- CBP
- Device class
- 2
- Regulation number
- 868.5870
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.