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FDA 510(k)

DM SLEEVE

K-Number: K021102 · 2002-05-08

ApplicantEmily Iker M.D., A.P.C.
Decision Date2002-05-08
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DM SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Emily Iker M.D., A.P.C.. It received FDA 510(k) clearance on 2002-05-08 under 510(k) number K021102. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DM SLEEVE?

DM SLEEVE is a medical device that received FDA 510(k) clearance on 2002-05-08. The listed applicant is Emily Iker M.D., A.P.C.. The 510(k) number is K021102.

When did DM SLEEVE receive FDA 510(k) clearance?

DM SLEEVE received FDA 510(k) clearance on 2002-05-08, under 510(k) number K021102.

Who is the listed applicant for DM SLEEVE?

The FDA 510(k) record lists Emily Iker M.D., A.P.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DM SLEEVE?

The FDA product code for DM SLEEVE is DWL.

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Related Devices (Code: DWL)

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.

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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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