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FDA 510(k)

BURRON CENTRAL VEIN CATHERIZATION KIT

K-Number: K810461 · 1981-03-11

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

Device Summary

BURRON CENTRAL VEIN CATHERIZATION KIT 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 K810461. 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 CENTRAL VEIN CATHERIZATION KIT?

BURRON CENTRAL VEIN CATHERIZATION KIT 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 K810461.

When did BURRON CENTRAL VEIN CATHERIZATION KIT receive FDA 510(k) clearance?

BURRON CENTRAL VEIN CATHERIZATION KIT received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810461.

Who is the listed applicant for BURRON CENTRAL VEIN CATHERIZATION KIT?

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 CENTRAL VEIN CATHERIZATION KIT?

The FDA product code for BURRON CENTRAL VEIN CATHERIZATION KIT is DQY.

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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.

K870403CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTUREK862412INTESTOPLANTK861479CAVAFIX, CENTRAL VENOUS CATHETER KITK860126STIMUPLEX, NERVE STIMULATORK851293IMPLANTOFIXK841428JEJUNOSTOMY SET FOR TUBE FEEDING

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Related Devices (Code: DQY)

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.

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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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