FDA 510(k)

CONTINUOUS FLUSH DEVICE

K-Number: K813549 · 1982-01-12

ApplicantNamic

Decision Date1982-01-12

Product CodeDRS

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CONTINUOUS FLUSH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Namic. It received FDA 510(k) clearance on 1982-01-12 under 510(k) number K813549. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTINUOUS FLUSH DEVICE?

CONTINUOUS FLUSH DEVICE is a medical device that received FDA 510(k) clearance on 1982-01-12. The listed applicant is Namic. The 510(k) number is K813549.

When did CONTINUOUS FLUSH DEVICE receive FDA 510(k) clearance?

CONTINUOUS FLUSH DEVICE received FDA 510(k) clearance on 1982-01-12, under 510(k) number K813549.

Who is the listed applicant for CONTINUOUS FLUSH DEVICE?

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

What is the FDA product code for CONTINUOUS FLUSH DEVICE?

The FDA product code for CONTINUOUS FLUSH DEVICE is DRS.

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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.