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FDA 510(k)

DISPOSABLE SUCKER SYSTEM

K-Number: K801400 · 1980-06-30

Decision Date1980-06-30
Product CodeDTS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SUCKER SYSTEM 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 K801400. The device is classified under product code DTS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SUCKER SYSTEM?

DISPOSABLE SUCKER SYSTEM 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 K801400.

When did DISPOSABLE SUCKER SYSTEM receive FDA 510(k) clearance?

DISPOSABLE SUCKER SYSTEM received FDA 510(k) clearance on 1980-06-30, under 510(k) number K801400.

Who is the listed applicant for DISPOSABLE SUCKER SYSTEM?

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 SUCKER SYSTEM?

The FDA product code for DISPOSABLE SUCKER SYSTEM is DTS.

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: DTS)

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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