MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS— 510(k) K030598

Name: FDA 510(k) clearance K030598
Creator: U.S. Food and Drug Administration
Published: 2004-01-23

Substantially Equivalent

Medisiss

FDA 510(k) clearance K030598 for MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS, Substantially Equivalent on 2004-01-23. Applicant: Medisiss. Device class: Unclassified.

Clearance details

Applicant: Medisiss
Product code: Code NLQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2003-02-25
Decision date: 2004-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sisters, OR, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NLQ

view all

K250898 — Reprocessed HARMONIC 700 Shears (3 models)2025-08-14
K241606 — Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm Length (HAR1120) +1 more2024-07-03
K233471 — Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm length (HAR1120) +1 more2024-02-20
K202554 — Reprocessed HARMONIC ACE+ 7, 5 mm Diameter Shears with Advanced Hemostasis2021-03-16
K193563 — Medline ReNewal Reprocessed Harmonic ACE+7 Shears2020-08-19

More clearances from Medisiss

view all

K113028 — MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS2011-12-20
K100543 — MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-012010-07-23
K081559 — GENESIS2008-08-28
K042659 — MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS2005-02-14
K030919 — SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES2003-07-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.