FDA 510(k)

QUICK FILL

K-Number: K800823 · 1980-04-29

Decision Date1980-04-29

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

QUICK FILL is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1980-04-29 under 510(k) number K800823. 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 QUICK FILL?

QUICK FILL is a medical device that received FDA 510(k) clearance on 1980-04-29. The listed applicant is Medrad, Inc.. The 510(k) number is K800823.

When did QUICK FILL receive FDA 510(k) clearance?

QUICK FILL received FDA 510(k) clearance on 1980-04-29, under 510(k) number K800823.

Who is the listed applicant for QUICK FILL?

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

What is the FDA product code for QUICK FILL?

The FDA product code for QUICK FILL 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.