QUICKAIR CHOKE RELIEVER, MODEL 59-001A
FDA 510(k) clearance DEN000004 · decided 2000-02-29
Clearance details
- K-number
- DEN000004
- Device name
- QUICKAIR CHOKE RELIEVER, MODEL 59-001A
- Applicant
- Maet Industries, Inc.
- Decision
- Unknown
- Date received
- 2000-01-28
- Decision date
- 2000-02-29
- Days to decision
- 32 days
- Clearance type
- Post-NSE
- Product code
- MZT
- Device class
- 2
- Regulation number
- 868.5115
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Mississauga, Ontario, CA
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.