510(k) DEN000004
- Device
- QUICKAIR CHOKE RELIEVER, MODEL 59-001A
- Applicant
- Maet Industries, Inc.
- 510(k) number
- DEN000004
- Product code
- MZT
- Decision
- Unknown (DENG)
- Decision date
- 2000-02-29
- Date received
- 2000-01-28
- Regulation
- 868.5115
- Classification name
- Device, Heimlich Maneuver Assist
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Post-NSE
- Third party reviewed
- N
Applicant Contact#
- Contact
- WAYNE WITBECK
- Address
- 4215 Renoak Ct. Mississauga, Ontario CA L5C 4K3 L5C 4K3
FDA Registration Numbers#
- 3022568093
Source Documents#
510(k) summary PDF not indicated by FDA