Medical Device Manufacturer · US , San Antonio , TX

Pan-America Hyperbarics, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2002
4
Total
4
Cleared
0
Denied

Pan-America Hyperbarics, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Antonio, US.

Historical record: 4 cleared submissions from 2002 to 2013. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Pan-America Hyperbarics, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pan-America Hyperbarics, Inc.
4 devices
1-4 of 4
Cleared Mar 26, 2013
VERSALVENT MODEL V1 HYPERBARIC CHAMBER VENTILATOR MODEL V1
K122560 · CBK
Anesthesiology · 216d
Cleared Oct 24, 2002
PAN-AMERICA HYPERBARICS, HYPERBARIC CHAMBER SYSTEM, MODEL PAH-M10+2
K021689 · CBF
Anesthesiology · 154d
Cleared Oct 24, 2002
PAN-AMERICA HYPERBARICS HYPERBARIC CHAMBER SYSTEM, MODEL PAH-M3+1
K021690 · CBF
Anesthesiology · 155d
Cleared Oct 24, 2002
PAN-AMERICA HYPERBARICS HYPERBARIC CHAMBER SYSTEM, MODEL PAH-S1
K021693 · CBF
Anesthesiology · 155d
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All4 Anesthesiology 4