Pan-America Hyperbarics, Inc. is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
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
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