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FDA 510(k)

J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T

K-Number: K951621 · 1995-06-22

ApplicantJ&S Associates
Decision Date1995-06-22
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T is the device name listed in this FDA 510(k) record. The listed applicant is J&S Associates. It received FDA 510(k) clearance on 1995-06-22 under 510(k) number K951621. 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 J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T?

J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is J&S Associates. The 510(k) number is K951621.

When did J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T receive FDA 510(k) clearance?

J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T received FDA 510(k) clearance on 1995-06-22, under 510(k) number K951621.

Who is the listed applicant for J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T?

The FDA 510(k) record lists J&S Associates as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T?

The FDA product code for J & S WHEELCHAIRS MODELS 500, 500B, 502, 503, 504 AND 500T is IOR.

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Related Devices (Code: 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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