The following data is part of a premarket notification filed by Stryker Sustainability Solutions with the FDA for Reprocessed Ligasure Curved, Small Jaw, Open Sealer/divider (lf1212a).
Device ID | K220411 |
510k Number | K220411 |
Device Name: | Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) |
Classification | Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed |
Applicant | Stryker Sustainability Solutions 1810 W Drake Drive Tempe, AZ 85283 |
Contact | Scott English |
Correspondent | Scott English Stryker Sustainability Solutions 1810 W Drake Drive Tempe, AZ 85283 |
Product Code | NUJ |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-02-14 |
Decision Date | 2022-05-13 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
57613327565305 | K220411 | 000 |