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FDA 510(k)

EPICAN EPIDURAL CANNULA, BEVEL ACCORD

K-Number: K813236 · 1981-12-03

ApplicantBurron Medical Products, Inc.
Decision Date1981-12-03
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EPICAN EPIDURAL CANNULA, BEVEL ACCORD 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 1981-12-03 under 510(k) number K813236. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPICAN EPIDURAL CANNULA, BEVEL ACCORD?

EPICAN EPIDURAL CANNULA, BEVEL ACCORD is a medical device that received FDA 510(k) clearance on 1981-12-03. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K813236.

When did EPICAN EPIDURAL CANNULA, BEVEL ACCORD receive FDA 510(k) clearance?

EPICAN EPIDURAL CANNULA, BEVEL ACCORD received FDA 510(k) clearance on 1981-12-03, under 510(k) number K813236.

Who is the listed applicant for EPICAN EPIDURAL CANNULA, BEVEL ACCORD?

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 EPICAN EPIDURAL CANNULA, BEVEL ACCORD?

The FDA product code for EPICAN EPIDURAL CANNULA, BEVEL ACCORD is BSP.

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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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