FDA 510(k)

CONTRAST INJECTION DEVICE

K-Number: K880877 · 1988-05-31

Decision Date1988-05-31

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CONTRAST INJECTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Med-West, Inc.. It received FDA 510(k) clearance on 1988-05-31 under 510(k) number K880877. 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 CONTRAST INJECTION DEVICE?

CONTRAST INJECTION DEVICE is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is Med-West, Inc.. The 510(k) number is K880877.

When did CONTRAST INJECTION DEVICE receive FDA 510(k) clearance?

CONTRAST INJECTION DEVICE received FDA 510(k) clearance on 1988-05-31, under 510(k) number K880877.

Who is the listed applicant for CONTRAST INJECTION DEVICE?

The FDA 510(k) record lists Med-West, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTRAST INJECTION DEVICE?

The FDA product code for CONTRAST INJECTION DEVICE is DXT.

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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.