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FDA 510(k)

RECLINING WHEELS

K-Number: K832511 · 1983-08-31

ApplicantReclining Wheels
Decision Date1983-08-31
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RECLINING WHEELS is the device name listed in this FDA 510(k) record. The listed applicant is Reclining Wheels. It received FDA 510(k) clearance on 1983-08-31 under 510(k) number K832511. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECLINING WHEELS?

RECLINING WHEELS is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Reclining Wheels. The 510(k) number is K832511.

When did RECLINING WHEELS receive FDA 510(k) clearance?

RECLINING WHEELS received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832511.

Who is the listed applicant for RECLINING WHEELS?

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

What is the FDA product code for RECLINING WHEELS?

The FDA product code for RECLINING WHEELS is INN.

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Related Devices (Code: INN)

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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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