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FDA 510(k)

LIFECARE MODEL 4 PUMP

K-Number: K900467 · 1990-08-27

ApplicantAbbott Laboratories
Decision Date1990-08-27
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFECARE MODEL 4 PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1990-08-27 under 510(k) number K900467. 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 LIFECARE MODEL 4 PUMP?

LIFECARE MODEL 4 PUMP is a medical device that received FDA 510(k) clearance on 1990-08-27. The listed applicant is Abbott Laboratories. The 510(k) number is K900467.

When did LIFECARE MODEL 4 PUMP receive FDA 510(k) clearance?

LIFECARE MODEL 4 PUMP received FDA 510(k) clearance on 1990-08-27, under 510(k) number K900467.

Who is the listed applicant for LIFECARE MODEL 4 PUMP?

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

What is the FDA product code for LIFECARE MODEL 4 PUMP?

The FDA product code for LIFECARE MODEL 4 PUMP is 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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