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FDA 510(k)

MTD HEDREST

K-Number: K884847 · 1989-01-09

ApplicantComposites Horizons, Inc.
Decision Date1989-01-09
Product CodeIWY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MTD HEDREST is the device name listed in this FDA 510(k) record. The listed applicant is Composites Horizons, Inc.. It received FDA 510(k) clearance on 1989-01-09 under 510(k) number K884847. The device is classified under product code IWY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTD HEDREST?

MTD HEDREST is a medical device that received FDA 510(k) clearance on 1989-01-09. The listed applicant is Composites Horizons, Inc.. The 510(k) number is K884847.

When did MTD HEDREST receive FDA 510(k) clearance?

MTD HEDREST received FDA 510(k) clearance on 1989-01-09, under 510(k) number K884847.

Who is the listed applicant for MTD HEDREST?

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

What is the FDA product code for MTD HEDREST?

The FDA product code for MTD HEDREST is IWY.

Related Clinical Trials

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Related Devices (Code: IWY)

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.

K925705ACCURAD-200 SYSTEM & ACCURAD-300 PLUS SYSTEMDenar Corp.K884493HEAD HOLDING DEVICE/SLEEP APNEAX-Ray SystemsK864527DUOCEPHGary E. Hall, DdsK850197KELLER CEPHALOMETRIC DEVICEGary D. KellerK844549HEAD-SPINE STABILIZER HSS-1Imaging Accessories, Inc.K843340PORTA-STATPorta-Stat, Inc.

Official Source

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

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