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FDA 510(k)

QUICK-CLIP NEEDLE GUIDE

K-Number: K903561 · 1991-03-05

ApplicantAcuson Corp.
Decision Date1991-03-05
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QUICK-CLIP NEEDLE GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Corp.. It received FDA 510(k) clearance on 1991-03-05 under 510(k) number K903561. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK-CLIP NEEDLE GUIDE?

QUICK-CLIP NEEDLE GUIDE is a medical device that received FDA 510(k) clearance on 1991-03-05. The listed applicant is Acuson Corp.. The 510(k) number is K903561.

When did QUICK-CLIP NEEDLE GUIDE receive FDA 510(k) clearance?

QUICK-CLIP NEEDLE GUIDE received FDA 510(k) clearance on 1991-03-05, under 510(k) number K903561.

Who is the listed applicant for QUICK-CLIP NEEDLE GUIDE?

The FDA 510(k) record lists Acuson Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICK-CLIP NEEDLE GUIDE?

The FDA product code for QUICK-CLIP NEEDLE GUIDE is ITX.

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Other records listing Acuson Corp. 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.

K023772KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEMK022896CSV12 SOFTWARE VIEWERK022567SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEMK021497CYPRESS ULTRASOUND SYSTEMK010950CYPRESS SYSTEMK0028073D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSING

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Related Devices (Code: ITX)

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.

K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna 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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