TOURIQUET KIT WITH SNARE— 510(k) K855144

Substantially Equivalent

Dlp, Inc.

FDA 510(k) clearance K855144 for TOURIQUET KIT WITH SNARE, Substantially Equivalent on 1986-02-05. Applicant: Dlp, Inc.. Device class: 1.

Clearance details

Applicant: Dlp, Inc.
Product code: Code GDJ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-12-26
Decision date: 1986-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Dlp, Inc.

K973485 — CLEARVIEW BLOWER/MISTER1997-12-08
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K953945 — RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLET1996-03-26
K950754 — MACRO SUCTION TUBE MODEL NO 100611995-04-25
K934215 — CONTAIN-OR1994-02-09

Recalls naming K855144

K-number listed on FDA's recall record

Z-2423-2024 — TourniKwik Tourniquet Set (CFN 79012)Class II·Ongoing·Medtronic Perfusion Systems·20240516

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K855144.

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