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FDA 510(k)

SIGHT-PLUS ARTHROSCOPE

K-Number: K925226 · 1993-07-28

ApplicantAmerican Medical Concepts, Inc.
Decision Date1993-07-28
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SIGHT-PLUS ARTHROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Concepts, Inc.. It received FDA 510(k) clearance on 1993-07-28 under 510(k) number K925226. 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 SIGHT-PLUS ARTHROSCOPE?

SIGHT-PLUS ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1993-07-28. The listed applicant is American Medical Concepts, Inc.. The 510(k) number is K925226.

When did SIGHT-PLUS ARTHROSCOPE receive FDA 510(k) clearance?

SIGHT-PLUS ARTHROSCOPE received FDA 510(k) clearance on 1993-07-28, under 510(k) number K925226.

Who is the listed applicant for SIGHT-PLUS ARTHROSCOPE?

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

What is the FDA product code for SIGHT-PLUS ARTHROSCOPE?

The FDA product code for SIGHT-PLUS ARTHROSCOPE 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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