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FDA 510(k)

BRACHIAL PLEXUS ANESTHESIA TRAY

K-Number: K840287 · 1984-02-23

Decision Date1984-02-23
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BRACHIAL PLEXUS ANESTHESIA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1984-02-23 under 510(k) number K840287. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRACHIAL PLEXUS ANESTHESIA TRAY?

BRACHIAL PLEXUS ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1984-02-23. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K840287.

When did BRACHIAL PLEXUS ANESTHESIA TRAY receive FDA 510(k) clearance?

BRACHIAL PLEXUS ANESTHESIA TRAY received FDA 510(k) clearance on 1984-02-23, under 510(k) number K840287.

Who is the listed applicant for BRACHIAL PLEXUS ANESTHESIA TRAY?

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

What is the FDA product code for BRACHIAL PLEXUS ANESTHESIA TRAY?

The FDA product code for BRACHIAL PLEXUS ANESTHESIA TRAY is CAZ.

Related Clinical Trials

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.

Other records listing Burron Medical Products, 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.

View all 41 devices →

Related Devices (Code: CAZ)

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.

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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