FDA 510(k)

MoistureMeterD Compact, LymphScanner

K-Number: K220557 · 2022-05-27

Decision Date2022-05-27

Product CodeOBH

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MoistureMeterD Compact, LymphScanner is the device name listed in this FDA 510(k) record. The listed applicant is Delfin Technologies, Ltd.. It received FDA 510(k) clearance on 2022-05-27 under 510(k) number K220557. The device is classified under product code OBH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MoistureMeterD Compact, LymphScanner?

MoistureMeterD Compact, LymphScanner is a medical device that received FDA 510(k) clearance on 2022-05-27. The listed applicant is Delfin Technologies, Ltd.. The 510(k) number is K220557.

When did MoistureMeterD Compact, LymphScanner receive FDA 510(k) clearance?

MoistureMeterD Compact, LymphScanner received FDA 510(k) clearance on 2022-05-27, under 510(k) number K220557.

Who is the listed applicant for MoistureMeterD Compact, LymphScanner?

The FDA 510(k) record lists Delfin Technologies, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MoistureMeterD Compact, LymphScanner?

The FDA product code for MoistureMeterD Compact, LymphScanner is OBH.

Related Devices (Code: OBH)

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.