Dhd Diemolding Healthcare Div.
Canastota, NY, US
Dhd Diemolding Healthcare Div. appears in FDA device records in Canastota, NY. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Dhd Diemolding Healthcare Div. between 1991 and 1998. The busiest year on record is 1992, with 3. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 1 |
| 1992 | 3 |
| 1993 | 1 |
| 1995 | 3 |
| 1996 | 1 |
| 1997 | 1 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K973532 | STEALTH, METERED DOSE INHALER (MDI) SPACER WITHOUT INTEGRAL ACTUATOR | CAF | Substantially Equivalent | |
| K970596 | DHD EMERALD PRODUCT | BWF | Substantially Equivalent | |
| K961973 | DHD ACE WITH MASK KIT | CAF | Substantially Equivalent | |
| K953206 | DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION) | CAF | Substantially Equivalent | |
| K945118 | EXPIRATORY BREATHING EXERCISER | BWF | Substantially Equivalent | |
| K944900 | THERAPEP | BWF | Substantially Equivalent | |
| K926301 | ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO | CAF | Substantially Equivalent | |
| K922537 | DURALIFE | BZA | Substantially Equivalent | |
| K913726 | DURALIFE(TM) | BZA | Substantially Equivalent | |
| K913326 | DHD METERED DOSE INHALER (MDI) SPACER | CAF | Substantially Equivalent | |
| K911294 | ULTRASET CATHETER | BZA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain