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FDA 510(k)

BURRON PERCUTANEOUS INDUCER SET

K-Number: K810460 · 1981-03-11

ApplicantBurron Medical Products, Inc.
Decision Date1981-03-11
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BURRON PERCUTANEOUS INDUCER SET 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 1981-03-11 under 510(k) number K810460. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURRON PERCUTANEOUS INDUCER SET?

BURRON PERCUTANEOUS INDUCER SET is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K810460.

When did BURRON PERCUTANEOUS INDUCER SET receive FDA 510(k) clearance?

BURRON PERCUTANEOUS INDUCER SET received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810460.

Who is the listed applicant for BURRON PERCUTANEOUS INDUCER SET?

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 BURRON PERCUTANEOUS INDUCER SET?

The FDA product code for BURRON PERCUTANEOUS INDUCER SET is DQY.

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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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