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FDA 510(k)

HORIZON SURGICAL LIGATING AND MARKING CLIP

K-Number: K901303 · 1990-06-05

ApplicantHorizon Surgical, Inc.
Decision Date1990-06-05
Product CodeDSS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HORIZON SURGICAL LIGATING AND MARKING CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Horizon Surgical, Inc.. It received FDA 510(k) clearance on 1990-06-05 under 510(k) number K901303. The device is classified under product code DSS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZON SURGICAL LIGATING AND MARKING CLIP?

HORIZON SURGICAL LIGATING AND MARKING CLIP is a medical device that received FDA 510(k) clearance on 1990-06-05. The listed applicant is Horizon Surgical, Inc.. The 510(k) number is K901303.

When did HORIZON SURGICAL LIGATING AND MARKING CLIP receive FDA 510(k) clearance?

HORIZON SURGICAL LIGATING AND MARKING CLIP received FDA 510(k) clearance on 1990-06-05, under 510(k) number K901303.

Who is the listed applicant for HORIZON SURGICAL LIGATING AND MARKING CLIP?

The FDA 510(k) record lists Horizon Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HORIZON SURGICAL LIGATING AND MARKING CLIP?

The FDA product code for HORIZON SURGICAL LIGATING AND MARKING CLIP is DSS.

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Related Devices (Code: DSS)

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.

K983744MCAS (MODULAR CLIP APPLIER SYSTEM)Applied Medical ResourcesK961333HEARTPORT MULTIFIRE CLIP APPLIERHeartport, Inc.K920104IDENTI LOOPS DEGANIA SILICONEPuritas Health Care, Inc.K920676RMI SOFCLAMPResearch Medical, Inc.K914523CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COILCatheter Research C/O Burditt, Bowles & RadziusK883909SURGICAL SPRING CLIPSApplied Vascular Devices, Inc.

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.

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