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FDA 510(k)

INJECTION FILL TUBE

K-Number: K823238 · 1982-12-30

ApplicantVetrex Medical Corp.
Decision Date1982-12-30
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INJECTION FILL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Vetrex Medical Corp.. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K823238. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTION FILL TUBE?

INJECTION FILL TUBE is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Vetrex Medical Corp.. The 510(k) number is K823238.

When did INJECTION FILL TUBE receive FDA 510(k) clearance?

INJECTION FILL TUBE received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823238.

Who is the listed applicant for INJECTION FILL TUBE?

The FDA 510(k) record lists Vetrex Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INJECTION FILL TUBE?

The FDA product code for INJECTION FILL TUBE is DXT.

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Related Devices (Code: DXT)

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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