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FDA 510(k)

SAPHENOUS VEIN CANNULAE

K-Number: K801396 · 1980-06-30

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

Device Summary

SAPHENOUS VEIN CANNULAE 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 K801396. 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 SAPHENOUS VEIN CANNULAE?

SAPHENOUS VEIN CANNULAE 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 K801396.

When did SAPHENOUS VEIN CANNULAE receive FDA 510(k) clearance?

SAPHENOUS VEIN CANNULAE received FDA 510(k) clearance on 1980-06-30, under 510(k) number K801396.

Who is the listed applicant for SAPHENOUS VEIN CANNULAE?

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 SAPHENOUS VEIN CANNULAE?

The FDA product code for SAPHENOUS VEIN CANNULAE 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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