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FDA 510(k)

SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM

K-Number: K960372 · 1996-04-26

ApplicantScanlan Intl., Inc.
Decision Date1996-04-26
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Scanlan Intl., Inc.. It received FDA 510(k) clearance on 1996-04-26 under 510(k) number K960372. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM?

SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM is a medical device that received FDA 510(k) clearance on 1996-04-26. The listed applicant is Scanlan Intl., Inc.. The 510(k) number is K960372.

When did SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM receive FDA 510(k) clearance?

SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM received FDA 510(k) clearance on 1996-04-26, under 510(k) number K960372.

Who is the listed applicant for SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM?

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

What is the FDA product code for SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM?

The FDA product code for SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM is HCH.

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Other records listing Scanlan Intl., Inc. as applicant

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.

K945474SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDERK911184SCANLAN/TAHERI VALVULOTOMEK864920SCANLAN (TM) INSTRUMENT TRAYK864919SCANLAN (TM) VEIN/GRAFT HOLDERK851825SCANLAN TUNNELER, SHEATH & TIPK841521SCANLAN ENDARSECTOR

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Related Devices (Code: HCH)

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.

K211183Sugita AVM MicroclipsMizuho America, Inc.K180757D-Clip; D-Clip ApplierPeter Lazic GmbHK091921CODMAN ANEURYSM CLIPS, CODMAN AVM MICRO CLIP SYSTEM, CODMAN SLIM-LINE GRAFT, REINFORCING, MINI ANEURYSM CLIPCodman & Shurtleff, Inc.K081640GIMMI ANEURYSM CLIPS AND APPLYING FORCEPSGimmi GmbHK081489L-ANEURYSM-CLIP SYSTEM & L-ANEURYSM CLIP APPLIERS, YASARGIL ANEURYSM CLIPS & YASARGIL ANEURYSM CLIP APPLIERSPeter Lazic GmbHK060915KIRWAN L-ANEURYSM CLIPS AND APPLIER, KIRWAN YASARGIL-TYPE ANEURYSM CLIPS AND APPLIERSKirwan Surgical Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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