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FDA 510(k)

MSD EMBOLECTOMY BASKET

K-Number: K991093 · 2000-12-21

ApplicantMetamorphic Surgical Devices, LLC
Decision Date2000-12-21
Product CodeQEW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MSD EMBOLECTOMY BASKET is the device name listed in this FDA 510(k) record. The listed applicant is Metamorphic Surgical Devices, LLC. It received FDA 510(k) clearance on 2000-12-21 under 510(k) number K991093. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSD EMBOLECTOMY BASKET?

MSD EMBOLECTOMY BASKET is a medical device that received FDA 510(k) clearance on 2000-12-21. The listed applicant is Metamorphic Surgical Devices, LLC. The 510(k) number is K991093.

When did MSD EMBOLECTOMY BASKET receive FDA 510(k) clearance?

MSD EMBOLECTOMY BASKET received FDA 510(k) clearance on 2000-12-21, under 510(k) number K991093.

Who is the listed applicant for MSD EMBOLECTOMY BASKET?

The FDA 510(k) record lists Metamorphic Surgical Devices, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSD EMBOLECTOMY BASKET?

The FDA product code for MSD EMBOLECTOMY BASKET is QEW.

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Related Devices (Code: QEW)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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