Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider— 510(k) K162751
Substantially EquivalentSurgical Instrument Services and Savings, Inc.
FDA 510(k) clearance K162751 for Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider, Substantially Equivalent on 2017-05-01. Applicant: Surgical Instrument Services and Savings, Inc.. Device class: 2.
Clearance details
- Applicant
- Surgical Instrument Services and Savings, Inc.
- Product code
- Code NUJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redmond, OR, US
Recent devices under product code NUJ
view all- K232511 — Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)
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- K220411 — Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
- K211203 — Green OR Reprocessed Aquamantys Bipolar Sealer
- K191073 — Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter
More clearances from Surgical Instrument Services and Savings, Inc.
view allRecalls naming K162751
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K162751.
Data sourced from openFDA. This site is unofficial and independent of the FDA.