Pancretec, Inc.
Walker, MI, US
Pancretec, Inc. appears in FDA device records in Walker, MI. 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 Pancretec, Inc. between 1984 and 1988. The busiest year on record is 1984, with 8. The most recent is 1988, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 8 |
| 1987 | 1 |
| 1988 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K882102 | PROVIDER ONE INFUSION SYSTEM | FRN | Substantially Equivalent | |
| K871806 | PROVIDER IV. MODEL 5000 INFUSION DEVICE | FRN | Substantially Equivalent | |
| K844078 | PROVIDER PA 3000 INFUSION SYSTEM | FRN | Substantially Equivalent | |
| K843463 | PROVIDER BAG SPIKE W/12 MICROBORE EXTEN | FPA | Substantially Equivalent | |
| K841373 | PROVIDER IV MODEL 2000 INFUSIN SYS | FRN | Substantially Equivalent | |
| K841017 | PROVIDER INFUSION SET | FRN | Substantially Equivalent | |
| K841027 | PROVIDER SITE PREP & CHECK STRIP KIT | FPA | Substantially Equivalent | |
| K833983 | PROVIDER U-100 INSULIN INFUSION SYS | FRN | Substantially Equivalent | |
| K841028 | PROVIDER CAP SET | FPA | Substantially Equivalent | |
| K841018 | PANCRETEC PUMP CHECK | FRN | 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