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FDA 510(k)

AMO ARTHOSCOPES

K-Number: K962330 · 1996-09-11

ApplicantAmerican Microptiks, Inc.
Decision Date1996-09-11
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AMO ARTHOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is American Microptiks, Inc.. It received FDA 510(k) clearance on 1996-09-11 under 510(k) number K962330. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMO ARTHOSCOPES?

AMO ARTHOSCOPES is a medical device that received FDA 510(k) clearance on 1996-09-11. The listed applicant is American Microptiks, Inc.. The 510(k) number is K962330.

When did AMO ARTHOSCOPES receive FDA 510(k) clearance?

AMO ARTHOSCOPES received FDA 510(k) clearance on 1996-09-11, under 510(k) number K962330.

Who is the listed applicant for AMO ARTHOSCOPES?

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

What is the FDA product code for AMO ARTHOSCOPES?

The FDA product code for AMO ARTHOSCOPES is HRX.

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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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