FDA 510(k) K230251, Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A), by Stryker Sustainability Solutions
FDA 510(k) K230251, Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A), by Stryker Sustainability Solutions
Device Classification Name: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
510(k) Number: K230251
Device Name: Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
Applicant: Stryker Sustainability Solutions
Regulation Number: 878.44
Classification Product Code: NUJ
Date Received: 2023-01-30
Decision Date: 2023-03-28
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
510k Review Panel: General & Plastic Surgery
Total number of pages: 527
Fully redacted pages: 390
Content pages: 137
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