TRANSFER CONTAINER HUMIDIFIER
FDA 510(k) clearance K881648 · decided 1988-12-30
Clearance details
- K-number
- K881648
- Device name
- TRANSFER CONTAINER HUMIDIFIER
- Applicant
- Newport Biosystems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-04-15
- Decision date
- 1988-12-30
- Days to decision
- 259 days
- Clearance type
- Traditional
- Product code
- CAF
- Device class
- 2
- Regulation number
- 868.5630
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Redwood City, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.