Pneupac, Ltd.
Waukesha, WI, US
Pneupac , Ltd. appears in FDA device records in Waukesha, WI. FDA records list 20 510(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
- 20
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 20 510(k) clearances for Pneupac, Ltd. between 1980 and 2004. The busiest year on record is 1980, with 9. The most recent is 2004, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 9 |
| 1982 | 1 |
| 1983 | 1 |
| 1984 | 1 |
| 1986 | 1 |
| 1987 | 1 |
| 1996 | 1 |
| 1998 | 1 |
| 2002 | 1 |
| 2003 | 2 |
| 2004 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K040090 | COMPPAC 200HD; CS12 POWER SUPPLY (AIRCRAFT/VECHILE); PS11 POWER SUPPLY (MAINS) | BTL | Substantially Equivalent | |
| K030803 | PARAPAC 200D TRANSPORT, MODEL V200D | BTL | Substantially Equivalent | |
| K021841 | COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGER | BTL | Substantially Equivalent | |
| K020899 | PARAPAC 200 MEDIC, MODEL P200, & PARAPAC 200D MEDIC, MODEL P200D | BTL | Substantially Equivalent | |
| K970158 | BABYPAC | CBK | Substantially Equivalent | |
| K960515 | PARAPAC | BTL | Substantially Equivalent | |
| K863410 | PATIENT VALVE WITH AIR ENTRAINMENT | BTL | Substantially Equivalent | |
| K862830 | MODELS 2R AND 3R PNEUPAC VENTILATOR/RESUSCITATOR | BTL | Substantially Equivalent | |
| K843737 | PNEUPAC INSTANT ACTION VENTILATOR/RESUS | CBK | Substantially Equivalent | |
| K832700 | PNEU PAC VENTILATOR/RESUSCITATORS | CBK | Substantially Equivalent | |
| K820220 | VENTILATOR MODELS | CBK | Substantially Equivalent | |
| K792459 | PNEUPAC VENTILATOR/RESUSCITATOR | CBK | Substantially Equivalent | |
| K792458 | PNEUPAC TEST SET, PT.#500-A250 | DRM | Substantially Equivalent | |
| K792457 | COMPRESSOR | BTI | Substantially Equivalent | |
| K792456 | PNEUPAC VENTILATOR/RESUSCITATOR #3 | CBK | Substantially Equivalent | |
| K792455 | PNEUPAC VENTILATOR/RESUSCITATOR #2 | CBK | Substantially Equivalent | |
| K792454 | PNEUPAC RESUSCITATOR INSTANT ACTION SET | DRM | Substantially Equivalent | |
| K792453 | PNEUPAC OXYGEN THERAPY UNIT | BTL | Substantially Equivalent | |
| K792452 | PNEUPAC RESUSCITATOR INSTANT ACTION SET | DRM | Substantially Equivalent | |
| K792451 | PNEUPAC RESUSCITATOR INSTANT ACTION SET | DRM | 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
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain