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FDA 510(k)

SUNDT SLIM-LINE ANEURYSM CLIP APPLIER

K-Number: K982379 · 1998-12-18

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1998-12-18
Product CodeHCI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SUNDT SLIM-LINE ANEURYSM CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K982379. The device is classified under product code HCI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNDT SLIM-LINE ANEURYSM CLIP APPLIER?

SUNDT SLIM-LINE ANEURYSM CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K982379.

When did SUNDT SLIM-LINE ANEURYSM CLIP APPLIER receive FDA 510(k) clearance?

SUNDT SLIM-LINE ANEURYSM CLIP APPLIER received FDA 510(k) clearance on 1998-12-18, under 510(k) number K982379.

Who is the listed applicant for SUNDT SLIM-LINE ANEURYSM CLIP APPLIER?

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

What is the FDA product code for SUNDT SLIM-LINE ANEURYSM CLIP APPLIER?

The FDA product code for SUNDT SLIM-LINE ANEURYSM CLIP APPLIER is HCI.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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Related Devices (Code: HCI)

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.

K221524Sugita AVM Microclip ApplierMizuho America, Inc.K211572Aesculap Slim Clip ApplierAesculap, Inc.K180914Aesculap Slim Clip ApplierAesculap, Inc.K173271Aesculap Slim Clip Applier ForcepsAesculap, Inc.K010910MEDICON YASARGIL CLIP APPLYING FORCEPSMedicon EGK994191SPETZLER ROUND HANDLE APPLIERS, MODELS C-3753, C-3753T, C-3754, C-3754TNmt Medical, 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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