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FDA 510(k)

PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR

K-Number: K884541 · 1988-11-23

ApplicantPro-Vertic, Inc.
Decision Date1988-11-23
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Vertic, Inc.. It received FDA 510(k) clearance on 1988-11-23 under 510(k) number K884541. 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 PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR?

PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1988-11-23. The listed applicant is Pro-Vertic, Inc.. The 510(k) number is K884541.

When did PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR receive FDA 510(k) clearance?

PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR received FDA 510(k) clearance on 1988-11-23, under 510(k) number K884541.

Who is the listed applicant for PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR?

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

What is the FDA product code for PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR?

The FDA product code for PRO-VERTIC 2000 STAND-UP/SELF-RISING WHEELCHAIR is IPL.

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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.

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