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FDA 510(k)

EVANS ARM AND HAND REST

K-Number: K760697 · 1976-11-02

ApplicantAlcon Laboratories
Decision Date1976-11-02
Product CodeHRK
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EVANS ARM AND HAND REST is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1976-11-02 under 510(k) number K760697. The device is classified under product code HRK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVANS ARM AND HAND REST?

EVANS ARM AND HAND REST is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is Alcon Laboratories. The 510(k) number is K760697.

When did EVANS ARM AND HAND REST receive FDA 510(k) clearance?

EVANS ARM AND HAND REST received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760697.

Who is the listed applicant for EVANS ARM AND HAND REST?

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

What is the FDA product code for EVANS ARM AND HAND REST?

The FDA product code for EVANS ARM AND HAND REST is HRK.

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Related Devices (Code: HRK)

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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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