Pan-America Hyperbarics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VERSALVENT MODEL V1 HYPERBARIC CHAMBER VENTILATOR MODEL V1, PAN-AMERICA HYPERBARICS, HYPERBARIC CHAMBER SYSTEM, MODEL PAH-M10+2, PAN-AMERICA HYPERBARICS HYPERBARIC CHAMBER SYSTEM, MODEL PAH-M3+1
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pan-America Hyperbarics, Inc. Anesthesiology ✕
4 devices
Cleared
Mar 26, 2013
VERSALVENT MODEL V1 HYPERBARIC CHAMBER VENTILATOR MODEL V1
Anesthesiology
216d
Cleared
Oct 24, 2002
PAN-AMERICA HYPERBARICS, HYPERBARIC CHAMBER SYSTEM, MODEL PAH-M10+2
Anesthesiology
154d
Cleared
Oct 24, 2002
PAN-AMERICA HYPERBARICS HYPERBARIC CHAMBER SYSTEM, MODEL PAH-M3+1
Anesthesiology
155d
Cleared
Oct 24, 2002
PAN-AMERICA HYPERBARICS HYPERBARIC CHAMBER SYSTEM, MODEL PAH-S1
Anesthesiology
155d