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FDA 510(k)

NAMIC CONTINUOUS FLUSH DEVICE

K-Number: K833271 · 1983-12-01

ApplicantNorth American Instrument Corp.
Decision Date1983-12-01
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NAMIC CONTINUOUS FLUSH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1983-12-01 under 510(k) number K833271. 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 NAMIC CONTINUOUS FLUSH DEVICE?

NAMIC CONTINUOUS FLUSH DEVICE is a medical device that received FDA 510(k) clearance on 1983-12-01. The listed applicant is North American Instrument Corp.. The 510(k) number is K833271.

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

NAMIC CONTINUOUS FLUSH DEVICE received FDA 510(k) clearance on 1983-12-01, under 510(k) number K833271.

Who is the listed applicant for NAMIC CONTINUOUS FLUSH DEVICE?

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

What is the FDA product code for NAMIC CONTINUOUS FLUSH DEVICE?

The FDA product code for NAMIC CONTINUOUS FLUSH DEVICE is DRS.

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Other records listing North American Instrument Corp. as applicant

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Related Devices (Code: 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.

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