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FDA 510(k)

STANDUP WHEELCHAIR

K-Number: K943337 · 1994-08-09

Decision Date1994-08-09
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STANDUP WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Nestor Rehab Products , Ltd.. It received FDA 510(k) clearance on 1994-08-09 under 510(k) number K943337. 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 STANDUP WHEELCHAIR?

STANDUP WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1994-08-09. The listed applicant is Nestor Rehab Products , Ltd.. The 510(k) number is K943337.

When did STANDUP WHEELCHAIR receive FDA 510(k) clearance?

STANDUP WHEELCHAIR received FDA 510(k) clearance on 1994-08-09, under 510(k) number K943337.

Who is the listed applicant for STANDUP WHEELCHAIR?

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

What is the FDA product code for STANDUP WHEELCHAIR?

The FDA product code for STANDUP WHEELCHAIR 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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