AcuSnare Polypectomy Snare - Duckbill
K-Number: K191048 · 2019-07-18
Device Summary
Frequently Asked Questions
What is the AcuSnare Polypectomy Snare - Duckbill?
AcuSnare Polypectomy Snare - Duckbill is a medical device that received FDA 510(k) clearance on 2019-07-18. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K191048.
When did AcuSnare Polypectomy Snare - Duckbill receive FDA 510(k) clearance?
AcuSnare Polypectomy Snare - Duckbill received FDA 510(k) clearance on 2019-07-18, under 510(k) number K191048.
Who is the listed applicant for AcuSnare Polypectomy Snare - Duckbill?
The FDA 510(k) record lists Wilson-Cook Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AcuSnare Polypectomy Snare - Duckbill?
The FDA product code for AcuSnare Polypectomy Snare - Duckbill is FDI.
Other records listing Wilson-Cook Medical, Inc. 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: FDI)
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.