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FDA 510(k)

INFUSION CONTROLLER, PARENTERAL

K-Number: K781216 · 1978-08-10

ApplicantNational Patent Development Corp.
Decision Date1978-08-10
Product CodeFLS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INFUSION CONTROLLER, PARENTERAL is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1978-08-10 under 510(k) number K781216. The device is classified under product code FLS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSION CONTROLLER, PARENTERAL?

INFUSION CONTROLLER, PARENTERAL is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is National Patent Development Corp.. The 510(k) number is K781216.

When did INFUSION CONTROLLER, PARENTERAL receive FDA 510(k) clearance?

INFUSION CONTROLLER, PARENTERAL received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781216.

Who is the listed applicant for INFUSION CONTROLLER, PARENTERAL?

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

What is the FDA product code for INFUSION CONTROLLER, PARENTERAL?

The FDA product code for INFUSION CONTROLLER, PARENTERAL is FLS.

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Other records listing National Patent Development Corp. as applicant

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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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