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FDA 510(k)

PERICAN, EPIDURAL CANNULA

K-Number: K813179 · 1981-12-03

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

Device Summary

PERICAN, EPIDURAL CANNULA 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 K813179. 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 PERICAN, EPIDURAL CANNULA?

PERICAN, EPIDURAL CANNULA 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 K813179.

When did PERICAN, EPIDURAL CANNULA receive FDA 510(k) clearance?

PERICAN, EPIDURAL CANNULA received FDA 510(k) clearance on 1981-12-03, under 510(k) number K813179.

Who is the listed applicant for PERICAN, EPIDURAL CANNULA?

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 PERICAN, EPIDURAL CANNULA?

The FDA product code for PERICAN, EPIDURAL CANNULA 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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