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FDA 510(k)

CAT 3040

K-Number: K830193 · 1983-03-09

Decision Date1983-03-09
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CAT 3040 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 1983-03-09 under 510(k) number K830193. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAT 3040?

CAT 3040 is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K830193.

When did CAT 3040 receive FDA 510(k) clearance?

CAT 3040 received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830193.

Who is the listed applicant for CAT 3040?

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 CAT 3040?

The FDA product code for CAT 3040 is KPE.

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: KPE)

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.

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