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FDA 510(k)

AMR-ACV CLAMPS

K-Number: K962668 · 1996-11-04

ApplicantApplied Medical Resources
Decision Date1996-11-04
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMR-ACV CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources. It received FDA 510(k) clearance on 1996-11-04 under 510(k) number K962668. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMR-ACV CLAMPS?

AMR-ACV CLAMPS is a medical device that received FDA 510(k) clearance on 1996-11-04. The listed applicant is Applied Medical Resources. The 510(k) number is K962668.

When did AMR-ACV CLAMPS receive FDA 510(k) clearance?

AMR-ACV CLAMPS received FDA 510(k) clearance on 1996-11-04, under 510(k) number K962668.

Who is the listed applicant for AMR-ACV CLAMPS?

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

What is the FDA product code for AMR-ACV CLAMPS?

The FDA product code for AMR-ACV CLAMPS is DXC.

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Other records listing Applied Medical Resources as applicant

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Related Devices (Code: DXC)

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.

K262086PreludeSYNC™ Radial Compression DeviceMerit Medical Systems, Inc.K260105Fogarty Spring Clips, Handleless Clamps, and Clamp InsertsEdwards LifesciencesK252772Arc Adjustable Radial Cuff Compression DeviceTz Medical, Inc.K254060Life Saving TourniquetTW MedicalK243627Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)Arc Trauma, LLCK253070Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)Medline Industries, LP

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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