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FDA 510(k)

BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION)

K-Number: K072475 · 2007-12-21

Decision Date2007-12-21
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION) is the device name listed in this FDA 510(k) record. The listed applicant is Etac Sverige AB. It received FDA 510(k) clearance on 2007-12-21 under 510(k) number K072475. 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 BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION)?

BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION) is a medical device that received FDA 510(k) clearance on 2007-12-21. The listed applicant is Etac Sverige AB. The 510(k) number is K072475.

When did BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION) receive FDA 510(k) clearance?

BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION) received FDA 510(k) clearance on 2007-12-21, under 510(k) number K072475.

Who is the listed applicant for BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION)?

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

What is the FDA product code for BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION)?

The FDA product code for BALDER FINESSE AND JUNIOR POWERED WHEELCHAIRS (WITH STAND-UP OPTION) 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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