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FDA 510(k)

HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES

K-Number: K022546 · 2002-08-12

ApplicantHorizons Intl. Corp.
Decision Date2002-08-12
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Horizons Intl. Corp.. It received FDA 510(k) clearance on 2002-08-12 under 510(k) number K022546. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES?

HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES is a medical device that received FDA 510(k) clearance on 2002-08-12. The listed applicant is Horizons Intl. Corp.. The 510(k) number is K022546.

When did HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES receive FDA 510(k) clearance?

HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES received FDA 510(k) clearance on 2002-08-12, under 510(k) number K022546.

Who is the listed applicant for HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES?

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

What is the FDA product code for HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES?

The FDA product code for HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES is EOQ.

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Other records listing Horizons Intl. Corp. as applicant

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Related Devices (Code: EOQ)

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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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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