FDA 510(k)

ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS

K-Number: K012640 · 2002-02-28

ApplicantMedical Instruments Technology, Inc.

Decision Date2002-02-28

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instruments Technology, Inc.. It received FDA 510(k) clearance on 2002-02-28 under 510(k) number K012640. 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 ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS?

ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS is a medical device that received FDA 510(k) clearance on 2002-02-28. The listed applicant is Medical Instruments Technology, Inc.. The 510(k) number is K012640.

When did ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS receive FDA 510(k) clearance?

ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS received FDA 510(k) clearance on 2002-02-28, under 510(k) number K012640.

Who is the listed applicant for ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS?

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

What is the FDA product code for ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS?

The FDA product code for ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS is HRX.

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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.