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FDA 510(k)

CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM

K-Number: K902374 · 1990-09-14

ApplicantPharmacia Deltec, Inc.
Decision Date1990-09-14
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1990-09-14 under 510(k) number K902374. 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 CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM?

CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 1990-09-14. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K902374.

When did CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM receive FDA 510(k) clearance?

CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM received FDA 510(k) clearance on 1990-09-14, under 510(k) number K902374.

Who is the listed applicant for CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM?

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

What is the FDA product code for CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM?

The FDA product code for CADD-TPN MODEL 5700 AMBULATORY INFUSION SYSTEM is FRN.

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Related Devices (Code: FRN)

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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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