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FDA 510(k)

VOLUMETRIC CONTROLLER MODEL 310

K-Number: K781589 · 1978-11-22

ApplicantImed Corp.
Decision Date1978-11-22
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VOLUMETRIC CONTROLLER MODEL 310 is the device name listed in this FDA 510(k) record. The listed applicant is Imed Corp.. It received FDA 510(k) clearance on 1978-11-22 under 510(k) number K781589. The device is classified under product code FLN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLUMETRIC CONTROLLER MODEL 310?

VOLUMETRIC CONTROLLER MODEL 310 is a medical device that received FDA 510(k) clearance on 1978-11-22. The listed applicant is Imed Corp.. The 510(k) number is K781589.

When did VOLUMETRIC CONTROLLER MODEL 310 receive FDA 510(k) clearance?

VOLUMETRIC CONTROLLER MODEL 310 received FDA 510(k) clearance on 1978-11-22, under 510(k) number K781589.

Who is the listed applicant for VOLUMETRIC CONTROLLER MODEL 310?

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

What is the FDA product code for VOLUMETRIC CONTROLLER MODEL 310?

The FDA product code for VOLUMETRIC CONTROLLER MODEL 310 is FLN.

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Other records listing Imed Corp. as applicant

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Related Devices (Code: FLN)

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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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