Medical Device Manufacturer · US , Canastota , NY

Dhd Diemolding Healthcare Div. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1991

Total

Cleared

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

1-11 of 11

Cleared Mar 19, 1998

STEALTH, METERED DOSE INHALER (MDI) SPACER WITHOUT INTEGRAL ACTUATOR

K973532 · CAF

Anesthesiology · 182d

DHD ACE WITH MASK KIT

K961973 · CAF

Anesthesiology · 87d

Cleared Aug 28, 1995

DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)

K953206 · CAF

Anesthesiology · 90d

Cleared Jan 13, 1995

EXPIRATORY BREATHING EXERCISER

ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO

K926301 · CAF

Anesthesiology · 218d

Cleared Dec 04, 1992

DURALIFE

K922537 · BZA

Anesthesiology · 190d

Cleared Feb 07, 1992

DURALIFE(TM)

K913726 · BZA

Anesthesiology · 171d

Cleared Jan 07, 1992

DHD METERED DOSE INHALER (MDI) SPACER

K913326 · CAF

Anesthesiology · 166d

Dhd Diemolding Healthcare Div. - FDA 510(k) Cleared Devices

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