FDA 510(k)

LTFS230

K-Number: K021775 · 2002-12-23

Decision Date2002-12-23

Product CodeLNS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

LTFS230 is the device name listed in this FDA 510(k) record. The listed applicant is Healthtronics, Inc.. It received FDA 510(k) clearance on 2002-12-23 under 510(k) number K021775. The device is classified under product code LNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LTFS230?

LTFS230 is a medical device that received FDA 510(k) clearance on 2002-12-23. The listed applicant is Healthtronics, Inc.. The 510(k) number is K021775.

When did LTFS230 receive FDA 510(k) clearance?

LTFS230 received FDA 510(k) clearance on 2002-12-23, under 510(k) number K021775.

Who is the listed applicant for LTFS230?

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

What is the FDA product code for LTFS230?

The FDA product code for LTFS230 is LNS.

Related Devices (Code: LNS)

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.