HORIZON SURGICAL LIGATING AND MARKING CLIP— 510(k) K901303

Name: FDA 510(k) clearance K901303
Creator: U.S. Food and Drug Administration
Published: 1990-06-05

Substantially Equivalent

Horizon Surgical, Inc.

FDA 510(k) clearance K901303 for HORIZON SURGICAL LIGATING AND MARKING CLIP, Substantially Equivalent on 1990-06-05. Applicant: Horizon Surgical, Inc.. Device class: 2.

Clearance details

Applicant: Horizon Surgical, Inc.
Product code: Code DSS
Device class: Class 2
Regulation: 21 CFR 870.3250
Advisory panel: Cardiovascular
Date received: 1990-03-20
Decision date: 1990-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Evergreen, CO, US

Download summary PDF View on FDA.gov ↗

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K983744 — MCAS (MODULAR CLIP APPLIER SYSTEM)1999-01-21
K961333 — HEARTPORT MULTIFIRE CLIP APPLIER1996-11-15
K920104 — IDENTI LOOPS DEGANIA SILICONE1992-04-20
K920676 — RMI SOFCLAMP1992-04-15
K914523 — CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COIL1992-01-10

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