Pari Innovative Manufacturers, Inc.
Midlothian, VA, US
Pari Innovative Manufacturers, Inc. appears in FDA device records in Midlothian, VA. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Pari Innovative Manufacturers, Inc. between 2002 and 2007. The busiest year on record is 2006, with 4. The most recent is 2007, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2002 | 1 |
| 2004 | 1 |
| 2006 | 4 |
| 2007 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K072670 | MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER | CAF | Substantially Equivalent | |
| K072982 | PARI HYDRATE V | BTT | Substantially Equivalent | |
| K070498 | HYPER SAL | CAF | Substantially Equivalent | |
| K070107 | PARI HYDRATE G | BTT | Substantially Equivalent | |
| K062158 | LC SPRINT STAR | CAF | Substantially Equivalent | |
| K061381 | LC STAR WITH NASAL ADAPTER | CAF | Substantially Equivalent | |
| K060357 | TREK S NEBULIZER COMPRESSOR | CAF | Substantially Equivalent | |
| K060399 | LC SPRINT NEBULIZER | CAF | Substantially Equivalent | |
| K033833 | EFLOW ELECTRONIC INHALER/NEBULIZER | CAF | Substantially Equivalent | |
| K020944 | VORTEX VALVED HOLDING CHAMBER | CAF | 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