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FDA 510(k)

R-MADE HEAD/ARM SUPPORT

K-Number: K923775 · 1992-10-20

ApplicantR-Made, Inc.
Decision Date1992-10-20
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

R-MADE HEAD/ARM SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is R-Made, Inc.. It received FDA 510(k) clearance on 1992-10-20 under 510(k) number K923775. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R-MADE HEAD/ARM SUPPORT?

R-MADE HEAD/ARM SUPPORT is a medical device that received FDA 510(k) clearance on 1992-10-20. The listed applicant is R-Made, Inc.. The 510(k) number is K923775.

When did R-MADE HEAD/ARM SUPPORT receive FDA 510(k) clearance?

R-MADE HEAD/ARM SUPPORT received FDA 510(k) clearance on 1992-10-20, under 510(k) number K923775.

Who is the listed applicant for R-MADE HEAD/ARM SUPPORT?

The FDA 510(k) record lists R-Made, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R-MADE HEAD/ARM SUPPORT?

The FDA product code for R-MADE HEAD/ARM SUPPORT is IXQ.

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Related Devices (Code: IXQ)

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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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