Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONTINUOUS EPIDURAL ANESTHES. TRAY

K-Number: K840179 · 1984-02-24

Decision Date1984-02-24
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS EPIDURAL ANESTHES. 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 1984-02-24 under 510(k) number K840179. 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 CONTINUOUS EPIDURAL ANESTHES. TRAY?

CONTINUOUS EPIDURAL ANESTHES. TRAY is a medical device that received FDA 510(k) clearance on 1984-02-24. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K840179.

When did CONTINUOUS EPIDURAL ANESTHES. TRAY receive FDA 510(k) clearance?

CONTINUOUS EPIDURAL ANESTHES. TRAY received FDA 510(k) clearance on 1984-02-24, under 510(k) number K840179.

Who is the listed applicant for CONTINUOUS EPIDURAL ANESTHES. 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 CONTINUOUS EPIDURAL ANESTHES. TRAY?

The FDA product code for CONTINUOUS EPIDURAL ANESTHES. 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.

↑