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FDA 510(k)

REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES

K-Number: K012536 · 2001-11-02

ApplicantSterilmed, Inc.
Decision Date2001-11-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2001-11-02 under 510(k) number K012536. 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 REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES?

REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES is a medical device that received FDA 510(k) clearance on 2001-11-02. The listed applicant is Sterilmed, Inc.. The 510(k) number is K012536.

When did REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES receive FDA 510(k) clearance?

REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES received FDA 510(k) clearance on 2001-11-02, under 510(k) number K012536.

Who is the listed applicant for REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES?

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

What is the FDA product code for REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES?

The FDA product code for REPROCESSED POWERED ARTHROSCOPIC ACCESSORIES 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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