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FDA 510(k)

ALTRACLUDE

K-Number: K811303 · 1981-06-16

ApplicantR&H Medical, Inc.
Decision Date1981-06-16
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALTRACLUDE is the device name listed in this FDA 510(k) record. The listed applicant is R&H Medical, Inc.. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811303. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTRACLUDE?

ALTRACLUDE is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is R&H Medical, Inc.. The 510(k) number is K811303.

When did ALTRACLUDE receive FDA 510(k) clearance?

ALTRACLUDE received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811303.

Who is the listed applicant for ALTRACLUDE?

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

What is the FDA product code for ALTRACLUDE?

The FDA product code for ALTRACLUDE is KDC.

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Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, 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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