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FDA 510(k)

MD2 PERSONAL INFUSION SYSTEM

K-Number: K896544 · 1990-05-02

ApplicantNorfolk Medical Products, Inc.
Decision Date1990-05-02
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MD2 PERSONAL INFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Medical Products, Inc.. It received FDA 510(k) clearance on 1990-05-02 under 510(k) number K896544. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MD2 PERSONAL INFUSION SYSTEM?

MD2 PERSONAL INFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K896544.

When did MD2 PERSONAL INFUSION SYSTEM receive FDA 510(k) clearance?

MD2 PERSONAL INFUSION SYSTEM received FDA 510(k) clearance on 1990-05-02, under 510(k) number K896544.

Who is the listed applicant for MD2 PERSONAL INFUSION SYSTEM?

The FDA 510(k) record lists Norfolk Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MD2 PERSONAL INFUSION SYSTEM?

The FDA product code for MD2 PERSONAL INFUSION SYSTEM is FRN.

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Other records listing Norfolk Medical Products, Inc. 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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