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FDA 510(k)

DISPOSABLE 2-STAGE CANNULA

K-Number: K810515 · 1981-04-23

ApplicantTexas Medical Products, Inc.
Decision Date1981-04-23
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE 2-STAGE CANNULA 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 1981-04-23 under 510(k) number K810515. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE 2-STAGE CANNULA?

DISPOSABLE 2-STAGE CANNULA is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Texas Medical Products, Inc.. The 510(k) number is K810515.

When did DISPOSABLE 2-STAGE CANNULA receive FDA 510(k) clearance?

DISPOSABLE 2-STAGE CANNULA received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810515.

Who is the listed applicant for DISPOSABLE 2-STAGE CANNULA?

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 2-STAGE CANNULA?

The FDA product code for DISPOSABLE 2-STAGE CANNULA is DWF.

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Related Devices (Code: DWF)

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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