FDA 510(k)

SHARP CHUTE

K-Number: K091690 · 2009-07-28

Decision Date2009-07-28

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SHARP CHUTE is the device name listed in this FDA 510(k) record. The listed applicant is Heathrow Scientific, LLC. It received FDA 510(k) clearance on 2009-07-28 under 510(k) number K091690. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARP CHUTE?

SHARP CHUTE is a medical device that received FDA 510(k) clearance on 2009-07-28. The listed applicant is Heathrow Scientific, LLC. The 510(k) number is K091690.

When did SHARP CHUTE receive FDA 510(k) clearance?

SHARP CHUTE received FDA 510(k) clearance on 2009-07-28, under 510(k) number K091690.

Who is the listed applicant for SHARP CHUTE?

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

What is the FDA product code for SHARP CHUTE?

The FDA product code for SHARP CHUTE is MMK.

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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.