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FDA 510(k)

ROLL A BOUT WALKER

K-Number: K941301 · 1994-05-02

ApplicantRoll A Bout Corp.
Decision Date1994-05-02
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ROLL A BOUT WALKER is the device name listed in this FDA 510(k) record. The listed applicant is Roll A Bout Corp.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K941301. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROLL A BOUT WALKER?

ROLL A BOUT WALKER is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Roll A Bout Corp.. The 510(k) number is K941301.

When did ROLL A BOUT WALKER receive FDA 510(k) clearance?

ROLL A BOUT WALKER received FDA 510(k) clearance on 1994-05-02, under 510(k) number K941301.

Who is the listed applicant for ROLL A BOUT WALKER?

The FDA 510(k) record lists Roll A Bout Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROLL A BOUT WALKER?

The FDA product code for ROLL A BOUT WALKER is IOR.

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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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