Weck Closure Systems
Research Triangle Park, NC, US
Weck Closure Systems appears in FDA device records in Research Triangle Park, NC. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Weck Closure Systems between 1998 and 2001. The busiest year on record is 1998, with 3. The most recent is 2001, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1998 | 3 |
| 1999 | 1 |
| 2000 | 1 |
| 2001 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K011660 | WECK CARDIAC PACING WIRES | LDF | Substantially Equivalent | |
| K003337 | HEM-O-LOK SMX, MODEL 544220; HEM-O-LOK ML, MODEL 544230; HEM-O-LOK MLX, MODEL 544240 | FZP | Substantially Equivalent | |
| K993157 | HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240 | FZP | Substantially Equivalent | |
| K982944 | HEM-O-LOCK, MODEL 523935 | FZP | Substantially Equivalent | |
| K982941 | HEM-O-LOK MODEL NUMBERS 523900, 523970 | FZP | Substantially Equivalent | |
| K982313 | HORIZON TITANIUM CLIPS, HORIZON TANTALUM CLIPS | FZP | 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