Healthdyne Technologies, Inc. is one of 20446 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Healthdyne Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SIMON MULTICHANNEL RECORDING SYSTEM, MODEL 5500, NASAL INTERFACE MODEL 7910, MODEL 7410 VOYAGER
9
Total
9
Cleared
0
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
Cleared
Mar 19, 1999
SIMON MULTICHANNEL RECORDING SYSTEM, MODEL 5500
Anesthesiology
157d
Cleared
Aug 04, 1998
NASAL INTERFACE MODEL 7910
Anesthesiology
252d
Cleared
Jun 29, 1998
MODEL 7410 VOYAGER
Anesthesiology
181d
Cleared
Jan 20, 1998
TWISTER OXYGEN CONCENTRATOR MODEL 600, TWISTER OXYGEN CONCENTRATOR W/OPI...
Anesthesiology
190d
Cleared
Aug 13, 1997
ALICE 4R SYSTEM
Neurology
85d
Cleared
Jul 25, 1997
PROTEGE LIQUID OXYGEN SYSTEM
Anesthesiology
88d
Cleared
Apr 16, 1997
MODEL 1700 TRANQUILITY BILEVEL SYSTEM
Anesthesiology
90d
Cleared
Feb 20, 1997
MODEL 7700 QUANTUM PRESSURE SUPPORT VENTILATOR PSV
Anesthesiology
238d
Cleared
Aug 05, 1994
7300 NASAL CPAP SYSTEM
Anesthesiology
16d