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FDA 510(k)

LSC, MODEL 3

K-Number: K061726 · 2006-12-04

ApplicantLifestand
Decision Date2006-12-04
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LSC, MODEL 3 is the device name listed in this FDA 510(k) record. The listed applicant is Lifestand. It received FDA 510(k) clearance on 2006-12-04 under 510(k) number K061726. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LSC, MODEL 3?

LSC, MODEL 3 is a medical device that received FDA 510(k) clearance on 2006-12-04. The listed applicant is Lifestand. The 510(k) number is K061726.

When did LSC, MODEL 3 receive FDA 510(k) clearance?

LSC, MODEL 3 received FDA 510(k) clearance on 2006-12-04, under 510(k) number K061726.

Who is the listed applicant for LSC, MODEL 3?

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

What is the FDA product code for LSC, MODEL 3?

The FDA product code for LSC, MODEL 3 is IPL.

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Other records listing Lifestand as applicant

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.

K042596LSA HELIUMK041535LSC LIFESTAND COMPACT

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Official Source

View on FDA Database →

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

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