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FDA 510(k)

AXIOM VESSEL LOOPS

K-Number: K800015 · 1980-03-25

ApplicantAxiom Medical, Inc.
Decision Date1980-03-25
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AXIOM VESSEL LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Axiom Medical, Inc.. It received FDA 510(k) clearance on 1980-03-25 under 510(k) number K800015. 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 AXIOM VESSEL LOOPS?

AXIOM VESSEL LOOPS is a medical device that received FDA 510(k) clearance on 1980-03-25. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K800015.

When did AXIOM VESSEL LOOPS receive FDA 510(k) clearance?

AXIOM VESSEL LOOPS received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800015.

Who is the listed applicant for AXIOM VESSEL LOOPS?

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

What is the FDA product code for AXIOM VESSEL LOOPS?

The FDA product code for AXIOM VESSEL LOOPS is KDC.

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Other records listing Axiom Medical, 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.

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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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