Ultrasonic Bipolar Generator USG-410 with accessories— 510(k) K211838

Substantially Equivalent

Olympus Medical Systems Corporation

FDA 510(k) clearance K211838 for Ultrasonic Bipolar Generator USG-410 with accessories, Substantially Equivalent on 2021-08-04. Applicant: Olympus Medical Systems Corporation. Device class: Unclassified.

Clearance details

Applicant
Olympus Medical Systems Corporation
Product code
Code LFL
Device class
Unclassified
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Hachioji-Shi, JP
Download summary PDFView on FDA.gov ↗

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Adverse events under product code LFL

product code LFL
Death
29
Injury
1,046
Malfunction
21,642
Total
22,717

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K211838

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K211838.

Data sourced from openFDA. This site is unofficial and independent of the FDA.