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FDA 510(k)

POWER STANDING DANI

K-Number: K090256 · 2009-07-06

Decision Date2009-07-06
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWER STANDING DANI is the device name listed in this FDA 510(k) record. The listed applicant is Davismade, Inc.. It received FDA 510(k) clearance on 2009-07-06 under 510(k) number K090256. 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 POWER STANDING DANI?

POWER STANDING DANI is a medical device that received FDA 510(k) clearance on 2009-07-06. The listed applicant is Davismade, Inc.. The 510(k) number is K090256.

When did POWER STANDING DANI receive FDA 510(k) clearance?

POWER STANDING DANI received FDA 510(k) clearance on 2009-07-06, under 510(k) number K090256.

Who is the listed applicant for POWER STANDING DANI?

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

What is the FDA product code for POWER STANDING DANI?

The FDA product code for POWER STANDING DANI is IPL.

Related Clinical Trials

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.

Related Devices (Code: IPL)

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.

Official Source

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