Healthdyne Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K983572 | SIMON MULTICHANNEL RECORDING SYSTEM, MODEL 5500 | March 19, 1999 |
| K974453 | NASAL INTERFACE MODEL 7910 | August 4, 1998 |
| K974879 | MODEL 7410 VOYAGER | June 29, 1998 |
| K972614 | TWISTER OXYGEN CONCENTRATOR MODEL 600, TWISTER OXYGEN CONCENTRATOR W/OPI MODEL 605 | January 20, 1998 |
| K971867 | ALICE 4R SYSTEM | August 13, 1997 |
| K971545 | PROTEGE LIQUID OXYGEN SYSTEM | July 25, 1997 |
| K970173 | MODEL 1700 TRANQUILITY BILEVEL SYSTEM | April 16, 1997 |
| K962517 | MODEL 7700 QUANTUM PRESSURE SUPPORT VENTILATOR PSV | February 20, 1997 |
| K943509 | 7300 NASAL CPAP SYSTEM | August 5, 1994 |