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FDA 510(k)

DISPOSABLE QUICK RELEASE PERFUSION ADAP

K-Number: K802544 · 1981-01-16

Decision Date1981-01-16
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE QUICK RELEASE PERFUSION ADAP 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 1981-01-16 under 510(k) number K802544. 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 DISPOSABLE QUICK RELEASE PERFUSION ADAP?

DISPOSABLE QUICK RELEASE PERFUSION ADAP is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is Texas Medical Products, Inc.. The 510(k) number is K802544.

When did DISPOSABLE QUICK RELEASE PERFUSION ADAP receive FDA 510(k) clearance?

DISPOSABLE QUICK RELEASE PERFUSION ADAP received FDA 510(k) clearance on 1981-01-16, under 510(k) number K802544.

Who is the listed applicant for DISPOSABLE QUICK RELEASE PERFUSION ADAP?

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 DISPOSABLE QUICK RELEASE PERFUSION ADAP?

The FDA product code for DISPOSABLE QUICK RELEASE PERFUSION ADAP is DTL.

Related Clinical Trials

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.

Other records listing Texas 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 30 devices →

Related Devices (Code: DTL)

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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