Medical Device Manufacturer · US , Pittston , PA

Penox Technologies, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1985

Total

Cleared

Denied

Penox Technologies, Inc. has 10 FDA 510(k) cleared medical devices. Based in Pittston, US.

Historical record: 10 cleared submissions from 1985 to 1987. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Penox Technologies, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Penox Technologies, Inc.

10 devices

1-10 of 10

Cleared Jan 21, 1987

PENOX HOSPITAL BED

K864667 · FNJ

General Hospital · 50d

Cleared Dec 15, 1986

PORTABLE LIQUID OXYGEN UNIT (MODIFICATION)

K863978 · BYJ

Anesthesiology · 62d

Cleared Jul 18, 1986

MODIFIED PENOX LIFT CHAIR

K862654 · INO

Physical Medicine · 7d

Cleared Nov 29, 1985

PENOX HIGH FLOW MANIFOLD

K853775 · BYJ

Anesthesiology · 80d

Cleared Aug 22, 1985

PENOX PERFORMER WHEELCHAIR

K852109 · IOR

Physical Medicine · 99d

Cleared Jun 21, 1985

PENOX LIFT CHAIR

K851218 · INO

Physical Medicine · 87d

Cleared Jun 18, 1985

T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTER

K851215 · CAM

Anesthesiology · 84d

Cleared Jun 18, 1985

PENOX DUAL FEED MANIFOLD

K851216 · CAM

Anesthesiology · 84d

Cleared Jun 18, 1985

PENOX DUAL FLOW MINIFOLD

K851217 · CAM

Anesthesiology · 84d

Cleared Jun 18, 1985

FILL HOSE SAFETY ADAPTER

K851219 · CAM

Anesthesiology · 84d

Penox Technologies, Inc. - FDA 510(k) Cleared Devices

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