Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device
K-Number: K212301 · 2021-11-15
Device Summary
Frequently Asked Questions
What is the Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device?
Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device is a medical device that received FDA 510(k) clearance on 2021-11-15. The listed applicant is Covidien, LLC. The 510(k) number is K212301.
When did Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device receive FDA 510(k) clearance?
Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device received FDA 510(k) clearance on 2021-11-15, under 510(k) number K212301.
Who is the listed applicant for Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device?
The FDA 510(k) record lists Covidien, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device?
The FDA product code for Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device is LFL.
Other records listing Covidien, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LFL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.