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FDA 510(k)

WALK-A-CYCLE

K-Number: K820711 · 1982-04-08

ApplicantWalk-A-Cycle Division
Decision Date1982-04-08
Product CodeITJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WALK-A-CYCLE is the device name listed in this FDA 510(k) record. The listed applicant is Walk-A-Cycle Division. It received FDA 510(k) clearance on 1982-04-08 under 510(k) number K820711. 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-A-CYCLE?

WALK-A-CYCLE is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is Walk-A-Cycle Division. The 510(k) number is K820711.

When did WALK-A-CYCLE receive FDA 510(k) clearance?

WALK-A-CYCLE received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820711.

Who is the listed applicant for WALK-A-CYCLE?

The FDA 510(k) record lists Walk-A-Cycle Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALK-A-CYCLE?

The FDA product code for WALK-A-CYCLE is ITJ.

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.

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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.K830784WALK N ROLLMeta-MorrisK830848RESI-WALKERLic-OrthionK823105RESI-WALKEROrthion Corp.K821404LIGHT WEIGHT ALUMINUM WALKERManuco Manufacturing Co., Inc.

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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