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FDA 510(k)

SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG

K-Number: K854737 · 1986-05-19

ApplicantOrthopaedic Devices , Ltd.
Decision Date1986-05-19
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG is the device name listed in this FDA 510(k) record. The listed applicant is Orthopaedic Devices , Ltd.. It received FDA 510(k) clearance on 1986-05-19 under 510(k) number K854737. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG?

SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG is a medical device that received FDA 510(k) clearance on 1986-05-19. The listed applicant is Orthopaedic Devices , Ltd.. The 510(k) number is K854737.

When did SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG receive FDA 510(k) clearance?

SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG received FDA 510(k) clearance on 1986-05-19, under 510(k) number K854737.

Who is the listed applicant for SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG?

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

What is the FDA product code for SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG?

The FDA product code for SURGICAL IRRIGATION DEVICE (SID)/ARTHROSCOPIC SURG is FQH.

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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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