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FDA 510(k)

DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID)

K-Number: K895686 · 1989-11-08

ApplicantStand-N-Go Corp.
Decision Date1989-11-08
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID) is the device name listed in this FDA 510(k) record. The listed applicant is Stand-N-Go Corp.. It received FDA 510(k) clearance on 1989-11-08 under 510(k) number K895686. 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 DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID)?

DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID) is a medical device that received FDA 510(k) clearance on 1989-11-08. The listed applicant is Stand-N-Go Corp.. The 510(k) number is K895686.

When did DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID) receive FDA 510(k) clearance?

DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID) received FDA 510(k) clearance on 1989-11-08, under 510(k) number K895686.

Who is the listed applicant for DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID)?

The FDA 510(k) record lists Stand-N-Go Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID)?

The FDA product code for DAILY ACTIVITY ASSIST DEVICE (MOBILE STANDING AID) 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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