Medical Device Manufacturer · US , Marietta , GA

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

9 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

Healthdyne Technologies, Inc. has 9 FDA 510(k) cleared medical devices. Based in Marietta, US.

Historical record: 9 cleared submissions from 1994 to 1999. Primary specialty: Anesthesiology.

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

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

9 devices

1-9 of 9

Cleared Mar 19, 1999

SIMON MULTICHANNEL RECORDING SYSTEM, MODEL 5500

K983572 · MNR

Anesthesiology · 157d

Cleared Aug 04, 1998

NASAL INTERFACE MODEL 7910

K974453 · BZD

Anesthesiology · 252d

Cleared Jun 29, 1998

MODEL 7410 VOYAGER

K974879 · BZD

Anesthesiology · 181d

Cleared Jan 20, 1998

TWISTER OXYGEN CONCENTRATOR MODEL 600, TWISTER OXYGEN CONCENTRATOR W/OPI...

K972614 · CAW

Anesthesiology · 190d

PROTEGE LIQUID OXYGEN SYSTEM

K971545 · BYJ

Anesthesiology · 88d

Cleared Apr 16, 1997

MODEL 1700 TRANQUILITY BILEVEL SYSTEM

K970173 · BZD

Anesthesiology · 90d

Cleared Feb 20, 1997

MODEL 7700 QUANTUM PRESSURE SUPPORT VENTILATOR PSV

K962517 · MNS

Anesthesiology · 238d

Cleared Aug 05, 1994

7300 NASAL CPAP SYSTEM

K943509 · BZD

Anesthesiology · 16d

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

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