NEWPORT COMMUNICAT PROTOCOL INTERFACE ADAPTOR
FDA 510(k) clearance K940739 · decided 1995-03-07
Clearance details
- K-number
- K940739
- Device name
- NEWPORT COMMUNICAT PROTOCOL INTERFACE ADAPTOR
- Applicant
- Newport Medical Instruments, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1994-02-17
- Decision date
- 1995-03-07
- Days to decision
- 383 days
- Clearance type
- Traditional
- Product code
- MOD
- Device class
- 2
- Regulation number
- 868.5895
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Costa Mesa, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.