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FDA 510(k)

RICHARD-ALLAN VESSEL LOOPS

K-Number: K900566 · 1990-05-03

ApplicantRichard-Allan Medical Ind., Inc.
Decision Date1990-05-03
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RICHARD-ALLAN VESSEL LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Richard-Allan Medical Ind., Inc.. It received FDA 510(k) clearance on 1990-05-03 under 510(k) number K900566. 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 RICHARD-ALLAN VESSEL LOOPS?

RICHARD-ALLAN VESSEL LOOPS is a medical device that received FDA 510(k) clearance on 1990-05-03. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K900566.

When did RICHARD-ALLAN VESSEL LOOPS receive FDA 510(k) clearance?

RICHARD-ALLAN VESSEL LOOPS received FDA 510(k) clearance on 1990-05-03, under 510(k) number K900566.

Who is the listed applicant for RICHARD-ALLAN VESSEL LOOPS?

The FDA 510(k) record lists Richard-Allan Medical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RICHARD-ALLAN VESSEL LOOPS?

The FDA product code for RICHARD-ALLAN VESSEL LOOPS is KDC.

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Other records listing Richard-Allan Medical Ind., 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.

K931879REFLEX HTRK924200REFLEX(R) ESCK926297REFLEX ESIK924761STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELDK896262TITANIUM LIGATING CLIPSK890314PROTECTOR (SURGICAL INSTRUMENT)

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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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