ClearanceBrief
Company ยท US

Dhd Diemolding Healthcare Div.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1998. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CAFNebulizer (Direct Patient Interface)5
BWFSpirometer, Therapeutic (Incentive)3
BZAConnector, Airway (Extension)3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 19, 1998K973532STEALTH, METERED DOSE INHALER (MDI) SPACER WITHOUT INTEGRAL ACTUATOR
Dhd Diemolding Healthcare Div.
CAF
May 16, 1997K970596DHD EMERALD PRODUCT
Dhd Diemolding Healthcare Div.
BWF
Aug 15, 1996K961973DHD ACE WITH MASK KIT
Dhd Diemolding Healthcare Div.
CAF
Aug 28, 1995K953206DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)
Dhd Diemolding Healthcare Div.
CAF
Jan 13, 1995K945118EXPIRATORY BREATHING EXERCISER
Dhd Diemolding Healthcare Div.
BWF
Jan 6, 1995K944900THERAPEP
Dhd Diemolding Healthcare Div.
BWF
Jul 21, 1993K926301ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO
Dhd Diemolding Healthcare Div.
CAF
Dec 4, 1992K922537DURALIFE
Dhd Diemolding Healthcare Div.
BZA
Feb 7, 1992K913726DURALIFE(TM)
Dhd Diemolding Healthcare Div.
BZA
Jan 7, 1992K913326DHD METERED DOSE INHALER (MDI) SPACER
Dhd Diemolding Healthcare Div.
CAF
Jun 10, 1991K911294ULTRASET CATHETER
Dhd Diemolding Healthcare Div.
BZA

Latest recalls

DateFirm and productCodeLinked 510(k)
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