Hemospray Endoscopic Hemostat
K-Number: K200972 · 2020-06-10
ApplicantWilson-Cook Medical, Inc.
Decision Date2020-06-10
Product CodeQAU
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Hemospray Endoscopic Hemostat is a medical device manufactured by Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2020-06-10 under approval number K200972. The device is classified under product code QAU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Hemospray Endoscopic Hemostat?
Hemospray Endoscopic Hemostat is a medical device that received FDA 510(k) clearance on 2020-06-10. It is manufactured by Wilson-Cook Medical, Inc.. The 510(k) number is K200972.
When was Hemospray Endoscopic Hemostat approved by the FDA?
Hemospray Endoscopic Hemostat received FDA 510(k) clearance on 2020-06-10, under approval number K200972.
What company makes Hemospray Endoscopic Hemostat?
Hemospray Endoscopic Hemostat is manufactured by Wilson-Cook Medical, Inc..
What is the FDA product code for Hemospray Endoscopic Hemostat?
The FDA product code for Hemospray Endoscopic Hemostat is QAU.
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Related Devices (Code: QAU)
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.