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FDA 510(k)

ARTHROSCOPIC TUBING SHEATH

K-Number: K896584 · 1989-12-27

ApplicantOrigin Medsystems, Inc.
Decision Date1989-12-27
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC TUBING SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1989-12-27 under 510(k) number K896584. 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 ARTHROSCOPIC TUBING SHEATH?

ARTHROSCOPIC TUBING SHEATH is a medical device that received FDA 510(k) clearance on 1989-12-27. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K896584.

When did ARTHROSCOPIC TUBING SHEATH receive FDA 510(k) clearance?

ARTHROSCOPIC TUBING SHEATH received FDA 510(k) clearance on 1989-12-27, under 510(k) number K896584.

Who is the listed applicant for ARTHROSCOPIC TUBING SHEATH?

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

What is the FDA product code for ARTHROSCOPIC TUBING SHEATH?

The FDA product code for ARTHROSCOPIC TUBING SHEATH is HRX.

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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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