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FDA 510(k)

DISPOSABLE ARTHROSCOPY CANNULA SET

K-Number: K813000 · 1982-01-22

ApplicantClinical Technology Corp.
Decision Date1982-01-22
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ARTHROSCOPY CANNULA SET is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K813000. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE ARTHROSCOPY CANNULA SET?

DISPOSABLE ARTHROSCOPY CANNULA SET is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Clinical Technology Corp.. The 510(k) number is K813000.

When did DISPOSABLE ARTHROSCOPY CANNULA SET receive FDA 510(k) clearance?

DISPOSABLE ARTHROSCOPY CANNULA SET received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813000.

Who is the listed applicant for DISPOSABLE ARTHROSCOPY CANNULA SET?

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

What is the FDA product code for DISPOSABLE ARTHROSCOPY CANNULA SET?

The FDA product code for DISPOSABLE ARTHROSCOPY CANNULA SET is LXH.

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Other records listing Clinical Technology Corp. as applicant

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Related Devices (Code: LXH)

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K192873SX-One MicroKnifeSonex Health, Inc.K101609SELF RETAINING SOFT TISSUE RETRACTORKoros USA, Inc.K001507MICROPERFORATION INSTRUMENTSmith & Nephew, Inc.K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMOrthopedic Systems, Inc.K943873ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SYOrthomet, Inc.K944188SPINAL MARKERLeibinger L.P.

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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