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FDA 510(k)

ULTRASONIC QFM SYSTEM 1000

K-Number: K811376 · 1981-08-13

ApplicantNarco Bio-Systems
Decision Date1981-08-13
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC QFM SYSTEM 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Narco Bio-Systems. It received FDA 510(k) clearance on 1981-08-13 under 510(k) number K811376. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASONIC QFM SYSTEM 1000?

ULTRASONIC QFM SYSTEM 1000 is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Narco Bio-Systems. The 510(k) number is K811376.

When did ULTRASONIC QFM SYSTEM 1000 receive FDA 510(k) clearance?

ULTRASONIC QFM SYSTEM 1000 received FDA 510(k) clearance on 1981-08-13, under 510(k) number K811376.

Who is the listed applicant for ULTRASONIC QFM SYSTEM 1000?

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

What is the FDA product code for ULTRASONIC QFM SYSTEM 1000?

The FDA product code for ULTRASONIC QFM SYSTEM 1000 is DPW.

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Other records listing Narco Bio-Systems as applicant

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Related Devices (Code: DPW)

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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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