Protek Medical Products, Inc.
Iowa City, IA, US
Protek Medical Products, Inc. appears in FDA device records in Iowa City, IA. 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 Protek Medical Products, Inc. between 1997 and 1998. The busiest year on record is 1997, with 8. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1997 | 8 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K973958 | GENERAL PURPOSE ATL NEEDLE GUIDE KIT | ITX | Substantially Equivalent | |
| K973622 | TRANSDUCER POSITIONER | ITX | Substantially Equivalent | |
| K970893 | ULTRASOUND TRANSDUCER DRAPE | FYA | Substantially Equivalent | |
| K970889 | ULTRASOUND TRANSDUCER DRAPE | KKX | Substantially Equivalent | |
| K973362 | NEEDLE GUIDE/GRID | ITX | Substantially Equivalent | |
| K970885 | ULTRASOUND SYSTEMS DRAPE | MMP | Substantially Equivalent | |
| K970891 | DRAPE, SURGICAL-LATEX | KKX | Substantially Equivalent | |
| K971722 | TRANS VAGINAL NEEDLE GUIDE | ITX | Substantially Equivalent | |
| K971115 | GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE | ITX | 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