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FDA 510(k)

MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS

K-Number: K042659 · 2005-02-14

ApplicantMedisiss
Decision Date2005-02-14
Product CodeNON
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Medisiss. It received FDA 510(k) clearance on 2005-02-14 under 510(k) number K042659. The device is classified under product code NON. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS?

MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 2005-02-14. The listed applicant is Medisiss. The 510(k) number is K042659.

When did MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS receive FDA 510(k) clearance?

MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS received FDA 510(k) clearance on 2005-02-14, under 510(k) number K042659.

Who is the listed applicant for MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS?

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 MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS?

The FDA product code for MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS is NON.

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.

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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#EIC8872-01K081559GENESISK030598MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTSK030919SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES

Related Devices (Code: NON)

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.

K042648REPROCESSED COLD BIOPSY FORCEPSSterilmed, Inc.K042594VANGUARD REPROCESSED NON-ELECTRIC BIOPSY FORCEPSVanguard Medical Concepts, Inc.

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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