HEMOCLIP SURGICAL OCCLUDING CLIP
FDA 510(k) clearance K800079 · decided 1980-01-28
Clearance details
- K-number
- K800079
- Device name
- HEMOCLIP SURGICAL OCCLUDING CLIP
- Applicant
- Edward Weck, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1980-01-14
- Decision date
- 1980-01-28
- Days to decision
- 14 days
- Clearance type
- Traditional
- Product code
- FZP
- Device class
- 2
- Regulation number
- 878.4300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Edward Weck
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| WECK Hemoclip Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended recall (Z-0826-2015) | Teleflex Medical | 2014-12-17 |