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FDA 510(k)

SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES

K-Number: K030919 · 2003-07-03

ApplicantMedisiss
Decision Date2003-07-03
Product CodeNLR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Medisiss. It received FDA 510(k) clearance on 2003-07-03 under 510(k) number K030919. The device is classified under product code NLR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES?

SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2003-07-03. The listed applicant is Medisiss. The 510(k) number is K030919.

When did SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES receive FDA 510(k) clearance?

SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES received FDA 510(k) clearance on 2003-07-03, under 510(k) number K030919.

Who is the listed applicant for SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES?

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

What is the FDA product code for SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES?

The FDA product code for SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES is NLR.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medisiss as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113028MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURSK100543MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01K081559GENESISK042659MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPSK030598MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS

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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