SURGICAL SPRING CLIPS— 510(k) K883909
Substantially EquivalentApplied Vascular Devices, Inc.
FDA 510(k) clearance K883909 for SURGICAL SPRING CLIPS, Substantially Equivalent on 1988-12-27. Applicant: Applied Vascular Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Applied Vascular Devices, Inc.
- Product code
- Code DSS
- Device class
- Class 2
- Regulation
- 21 CFR 870.3250
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Ana, CA, US
Recent devices under product code DSS
view allMore clearances from Applied Vascular Devices, Inc.
view allRecalls naming K883909
K-number listed on FDA's recall record- Z-2034-2020 — STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.
- Z-2035-2020 — STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.
- Z-2036-2020 — STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.
- Z-2037-2020 — STEALTH SPRING CLIP 6mm latis (1/4 Force). Non-Sterile, REF/UDI::A1702/(01)10607915110649 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K883909.
Data sourced from openFDA. This site is unofficial and independent of the FDA.