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FDA 510(k)

RICHARDS INTRA-ARTICULAR SHAVER MOTOR

K-Number: K842475 · 1984-09-17

Decision Date1984-09-17
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RICHARDS INTRA-ARTICULAR SHAVER MOTOR is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1984-09-17 under 510(k) number K842475. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICHARDS INTRA-ARTICULAR SHAVER MOTOR?

RICHARDS INTRA-ARTICULAR SHAVER MOTOR is a medical device that received FDA 510(k) clearance on 1984-09-17. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K842475.

When did RICHARDS INTRA-ARTICULAR SHAVER MOTOR receive FDA 510(k) clearance?

RICHARDS INTRA-ARTICULAR SHAVER MOTOR received FDA 510(k) clearance on 1984-09-17, under 510(k) number K842475.

Who is the listed applicant for RICHARDS INTRA-ARTICULAR SHAVER MOTOR?

The FDA 510(k) record lists Richards Medical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RICHARDS INTRA-ARTICULAR SHAVER MOTOR?

The FDA product code for RICHARDS INTRA-ARTICULAR SHAVER MOTOR is GEY.

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.

Other records listing Richards Medical Co., Inc. as applicant

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.

View all 71 devices →

Related Devices (Code: GEY)

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.

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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