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FDA 510(k)

CORONARY PERFUSION CONNECTOR PLUG

K-Number: K801399 · 1980-06-30

ApplicantTexas Medical Products, Inc.
Decision Date1980-06-30
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORONARY PERFUSION CONNECTOR PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Texas Medical Products, Inc.. It received FDA 510(k) clearance on 1980-06-30 under 510(k) number K801399. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORONARY PERFUSION CONNECTOR PLUG?

CORONARY PERFUSION CONNECTOR PLUG is a medical device that received FDA 510(k) clearance on 1980-06-30. The listed applicant is Texas Medical Products, Inc.. The 510(k) number is K801399.

When did CORONARY PERFUSION CONNECTOR PLUG receive FDA 510(k) clearance?

CORONARY PERFUSION CONNECTOR PLUG received FDA 510(k) clearance on 1980-06-30, under 510(k) number K801399.

Who is the listed applicant for CORONARY PERFUSION CONNECTOR PLUG?

The FDA 510(k) record lists Texas Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORONARY PERFUSION CONNECTOR PLUG?

The FDA product code for CORONARY PERFUSION CONNECTOR PLUG is DTL.

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Related Devices (Code: DTL)

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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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