Medical device licence · 23610 · Class 3
HYPERTEC HYPERBARIC CHAMBERS
No longer licensed: cancelled: quality-system requirement (2003)
Licence status Cancelled: quality-system requirement (2003); first licensed September 18, 2000; ended February 16, 2004. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 23610
- Licence holder
- Hypertec, Inc.Olney, TX, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Family
- First licensed
- September 18, 2000
- Ended
- February 16, 2004
- Devices covered
- 4
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- HYPERTEC DUOLOCK HYPERBARIC CHAMBER
- HYPERTEC MODEL 2500 HYBRID CHAMBER
- HYPERTEC MODEL 3200 HYBRID CHAMBER
- HYPERTEC MODEL 4200 MONOLECK CHAMBER
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.