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FDA 510(k)

WALK N ROLL

K-Number: K830784 · 1983-05-25

ApplicantMeta-Morris
Decision Date1983-05-25
Product CodeITJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WALK N ROLL is the device name listed in this FDA 510(k) record. The listed applicant is Meta-Morris. It received FDA 510(k) clearance on 1983-05-25 under 510(k) number K830784. The device is classified under product code ITJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALK N ROLL?

WALK N ROLL is a medical device that received FDA 510(k) clearance on 1983-05-25. The listed applicant is Meta-Morris. The 510(k) number is K830784.

When did WALK N ROLL receive FDA 510(k) clearance?

WALK N ROLL received FDA 510(k) clearance on 1983-05-25, under 510(k) number K830784.

Who is the listed applicant for WALK N ROLL?

The FDA 510(k) record lists Meta-Morris as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALK N ROLL?

The FDA product code for WALK N ROLL is ITJ.

Related Devices (Code: ITJ)

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.

K833869CHILD'S WALKERKaye Products, Inc.K833195UMBRELLA WALKERConvaid Products, Inc.K830848RESI-WALKERLic-OrthionK823105RESI-WALKEROrthion Corp.K821404LIGHT WEIGHT ALUMINUM WALKERManuco Manufacturing Co., Inc.K820711WALK-A-CYCLEWalk-A-Cycle Division

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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