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FDA 510(k)

VIDEO ARTHROSCOPE, 1.7MM X 55 MM

K-Number: K873387 · 1987-11-25

Decision Date1987-11-25
Product CodeHXR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIDEO ARTHROSCOPE, 1.7MM X 55 MM is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1987-11-25 under 510(k) number K873387. The device is classified under product code HXR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO ARTHROSCOPE, 1.7MM X 55 MM?

VIDEO ARTHROSCOPE, 1.7MM X 55 MM is a medical device that received FDA 510(k) clearance on 1987-11-25. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873387.

When did VIDEO ARTHROSCOPE, 1.7MM X 55 MM receive FDA 510(k) clearance?

VIDEO ARTHROSCOPE, 1.7MM X 55 MM received FDA 510(k) clearance on 1987-11-25, under 510(k) number K873387.

Who is the listed applicant for VIDEO ARTHROSCOPE, 1.7MM X 55 MM?

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

What is the FDA product code for VIDEO ARTHROSCOPE, 1.7MM X 55 MM?

The FDA product code for VIDEO ARTHROSCOPE, 1.7MM X 55 MM is HXR.

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 Arthropedics, 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 29 devices →

Related Devices (Code: HXR)

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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