Medi-Plast Intl., Inc.
Mchenry, IL, US
Medi-Plast Intl., Inc. appears in FDA device records in Mchenry, IL. FDA records list 12 510(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
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Medi-Plast Intl., Inc. between 1981 and 1996. The busiest year on record is 1981, with 4. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 4 |
| 1984 | 3 |
| 1985 | 1 |
| 1986 | 2 |
| 1987 | 1 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K954284 | MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON) | DTL | Substantially Equivalent | |
| K873588 | 10CC CONTROL SYRINGE | FMF | Substantially Equivalent | |
| K863402 | MEDI-PLAST DISPOSABLE MANIFOLD | DTL | Substantially Equivalent | |
| K861785 | FLUOROSCOPE BAND BAG | JAA | Substantially Equivalent | |
| K851489 | ARTERIAL-VENOUS COMPRESSION DRESSING | Substantially Equivalent | ||
| K842136 | STERILE PAN SET | FRG | Substantially Equivalent | |
| K840021 | OPERATING ROOM TRAY SET | FSM | Substantially Equivalent | |
| K840022 | HEART CATHETERIZATION TRAY SET | DRE | Substantially Equivalent | |
| K811268 | BOTTLE-TO-BOTTLE | KPE | Substantially Equivalent | |
| K811234 | I.V. BOTTLE (RIDGID) | KPE | Substantially Equivalent | |
| K811233 | I.V. PLASTIC BAG | KPE | Substantially Equivalent | |
| K811269 | GLASS VIALS | KPE | 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