Dhd Diemolding Healthcare Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dhd Diemolding Healthcare Div. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Dhd Diemolding Healthcare Div. has 11 FDA 510(k) cleared anesthesiology devices. Based in Canastota, US.
Historical record: 11 cleared submissions from 1991 to 1998.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dhd Diemolding Healthcare Div.
11 devices
Cleared
Mar 19, 1998
STEALTH, METERED DOSE INHALER (MDI) SPACER WITHOUT INTEGRAL ACTUATOR
Anesthesiology
182d
Cleared
May 16, 1997
DHD EMERALD PRODUCT
Anesthesiology
87d
Cleared
Aug 15, 1996
DHD ACE WITH MASK KIT
Anesthesiology
87d
Cleared
Aug 28, 1995
DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)
Anesthesiology
90d
Cleared
Jan 13, 1995
EXPIRATORY BREATHING EXERCISER
Anesthesiology
87d
Cleared
Jan 06, 1995
THERAPEP
Anesthesiology
94d
Cleared
Jul 21, 1993
ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO
Anesthesiology
218d
Cleared
Dec 04, 1992
DURALIFE
Anesthesiology
190d
Cleared
Feb 07, 1992
DURALIFE(TM)
Anesthesiology
171d
Cleared
Jan 07, 1992
DHD METERED DOSE INHALER (MDI) SPACER
Anesthesiology
166d
Cleared
Jun 10, 1991
ULTRASET CATHETER
Anesthesiology
77d