Pilling Weck Surgical
Fort Washington, PA, US
Pilling Weck Surgical appears in FDA device records in Fort Washington, PA. FDA records list 5 510(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
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Pilling Weck Surgical between 1998 and 2000. The busiest year on record is 1999, with 2. The most recent is 2000, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1998 | 1 |
| 1999 | 2 |
| 2000 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K992476 | PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS | MWS | Substantially Equivalent | |
| K992174 | PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP | DXC | Substantially Equivalent | |
| K990935 | JACKSON ESOPHAGEAL DILATOR | KNQ | Substantially Equivalent | |
| K990561 | OPTICAL FORCEPS | JEK | Substantially Equivalent | |
| K982128 | SHIKANI-FRENCH SPEAKING VALVE | JOH | 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