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FDA 510(k)

ARTHOSCOPE AND ACCESSORIES

K-Number: K931076 · 1994-03-31

ApplicantMeditron Devices, Inc.
Decision Date1994-03-31
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHOSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Meditron Devices, Inc.. It received FDA 510(k) clearance on 1994-03-31 under 510(k) number K931076. 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 ARTHOSCOPE AND ACCESSORIES?

ARTHOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-03-31. The listed applicant is Meditron Devices, Inc.. The 510(k) number is K931076.

When did ARTHOSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

ARTHOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1994-03-31, under 510(k) number K931076.

Who is the listed applicant for ARTHOSCOPE AND ACCESSORIES?

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

What is the FDA product code for ARTHOSCOPE AND ACCESSORIES?

The FDA product code for ARTHOSCOPE AND ACCESSORIES is HRX.

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Other records listing Meditron Devices, Inc. as applicant

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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.

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Official Source

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