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FDA 510(k)

CADD-PCA MODEL 5800 AMBULATORY INFUSION PUMP

K-Number: K890062 · 1989-03-23

ApplicantPharmacia Deltec, Inc.
Decision Date1989-03-23
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CADD-PCA MODEL 5800 AMBULATORY INFUSION PUMP 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 1989-03-23 under 510(k) number K890062. 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-PCA MODEL 5800 AMBULATORY INFUSION PUMP?

CADD-PCA MODEL 5800 AMBULATORY INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1989-03-23. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K890062.

When did CADD-PCA MODEL 5800 AMBULATORY INFUSION PUMP receive FDA 510(k) clearance?

CADD-PCA MODEL 5800 AMBULATORY INFUSION PUMP received FDA 510(k) clearance on 1989-03-23, under 510(k) number K890062.

Who is the listed applicant for CADD-PCA MODEL 5800 AMBULATORY INFUSION PUMP?

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-PCA MODEL 5800 AMBULATORY INFUSION PUMP?

The FDA product code for CADD-PCA MODEL 5800 AMBULATORY INFUSION PUMP 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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