Pharma-Plast USA, Inc.
Canada H3a 2n4, CA
Pharma-Plast USA, Inc. appears in FDA device records in Canada H3a 2n4, CA. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Pharma-Plast USA, Inc. between 1985 and 1989. The busiest year on record is 1989, with 5. The most recent is 1989, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 3 |
| 1987 | 1 |
| 1989 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K894371 | NIPRO SAFELET CATH | FOZ | Substantially Equivalent | |
| K894373 | NIPRO DENTAL NEEDLE | DZM | Substantially Equivalent | |
| K894374 | BLOOD DRAWING NEEDLE | FMI | Substantially Equivalent | |
| K894372 | NIPRO NEEDLE HOLDER | FMI | Substantially Equivalent | |
| K884978 | PHARMA-PLAST INSULIN INFUSION SET | LZG | Substantially Equivalent | |
| K871263 | MULTIPLE PHARMA-PLAST TRACHEAL TUBE | BTR | Substantially Equivalent | |
| K852444 | ASIK 'ONCE' SYRINGE | FMF | Substantially Equivalent | |
| K852443 | PHARMA-PLAST CLINIPAK | FMF | Substantially Equivalent | |
| K852442 | PHARMA-PLAST NEEDLE | FMI | 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