QUICKAIR CHOKE RELIEVER, MODEL 59-001A— 510(k) DEN000004
UnknownMaet Industries, Inc.
FDA 510(k) clearance DEN000004 for QUICKAIR CHOKE RELIEVER, MODEL 59-001A, Unknown on 2000-02-29. Applicant: Maet Industries, Inc.. Device class: 2.
Clearance details
- Applicant
- Maet Industries, Inc.
- Product code
- Code MZT
- Device class
- Class 2
- Regulation
- 21 CFR 868.5115
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Mississauga, Ontario, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.