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FDA 510(k)

ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX

K-Number: K093977 · 2010-04-22

ApplicantChestnut Medical Technologies, Inc.
Decision Date2010-04-22
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX is the device name listed in this FDA 510(k) record. The listed applicant is Chestnut Medical Technologies, Inc.. It received FDA 510(k) clearance on 2010-04-22 under 510(k) number K093977. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX?

ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX is a medical device that received FDA 510(k) clearance on 2010-04-22. The listed applicant is Chestnut Medical Technologies, Inc.. The 510(k) number is K093977.

When did ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX receive FDA 510(k) clearance?

ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX received FDA 510(k) clearance on 2010-04-22, under 510(k) number K093977.

Who is the listed applicant for ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX?

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

What is the FDA product code for ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX?

The FDA product code for ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX is DQY.

Related Clinical Trials

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.

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Other records listing Chestnut Medical Technologies, 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.

K091559MARKSMANN CATHETERK043580ALLIGATOR RETRIEVAL DEVICE (ARD)

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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