Respironics Inc., Sleep & Home Respiratory Group is one of 5577 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Respironics Inc., Sleep & Home Respiratory Group - FDA 510(k) Cleared...
Recent clearances: COMFORTGEL NASAL MASK, RESPIRONICS PERFORMAX SE TOTAL FACE MASK, BIPAP AUTOSV ADVANCED
21
Total
21
Cleared
0
Denied
Respironics Inc., Sleep & Home Respiratory Group has 21 FDA 510(k) cleared anesthesiology devices. Based in Murrysville, US.
Historical record: 21 cleared submissions from 2007 to 2010.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Respironics Inc., Sleep & Home Respiratory Group
21 devices
Cleared
Feb 12, 2010
COMFORTGEL NASAL MASK
Anesthesiology
150d
Cleared
Dec 18, 2009
RESPIRONICS PERFORMAX SE TOTAL FACE MASK
Anesthesiology
112d
Cleared
Oct 30, 2009
BIPAP AUTOSV ADVANCED
Anesthesiology
245d
Cleared
Oct 23, 2009
GAS TRANSFILL
Anesthesiology
183d
Cleared
Sep 10, 2009
COMFORT TWIN NASAL MASK
Anesthesiology
80d
Cleared
Sep 03, 2009
COMFORT TWIN NASAL MASK
Anesthesiology
142d
Cleared
Aug 03, 2009
REMSTAR AUTO A-FLEX
Anesthesiology
90d
Cleared
Jun 26, 2009
ALICE PDX
Anesthesiology
121d
Cleared
May 29, 2009
RESPIRONICS PERFORMAX TOTAL FACE MASK
Anesthesiology
29d
Cleared
May 08, 2009
REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM
Anesthesiology
95d
Cleared
Mar 13, 2009
TRILOGY 100 VENTILATOR
Anesthesiology
105d
Cleared
Mar 04, 2009
BIPAP AUTOSV
Anesthesiology
30d