FDA 510(k)

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

K-Number: K031869 · 2003-12-24

ApplicantSurgical Instruments Service and Savings, Inc.

Decision Date2003-12-24

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SISS INC. (D.B.A. MEDISISS) REPROCESSED ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instruments Service and Savings, Inc.. It received FDA 510(k) clearance on 2003-12-24 under 510(k) number K031869. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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

SISS INC. (D.B.A. MEDISISS) REPROCESSED ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2003-12-24. The listed applicant is Surgical Instruments Service and Savings, Inc.. The 510(k) number is K031869.

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

SISS INC. (D.B.A. MEDISISS) REPROCESSED ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES received FDA 510(k) clearance on 2003-12-24, under 510(k) number K031869.

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

The FDA 510(k) record lists Surgical Instruments Service and Savings, Inc. 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) REPROCESSED ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES?

The FDA product code for SISS INC. (D.B.A. MEDISISS) REPROCESSED ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES is GEI.

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Other records listing Surgical Instruments Service and Savings, Inc. as applicant

K030179MEDISISS PHACOEMULSIFICATION TIPS/NEEDLES K024011SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIES K012644REPROCESSED TROCARS AND CANNULAS K012669REPROCESSED ELECTROSURGICAL ELECTRODES K012667REPROCESSED ARTHROSCOPIC SHAPERS K012658REPROCESSED COMPRESSION LIMB SLEEVES

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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.