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FDA 510(k)

ABBOTT LIFECARE 500 INFUSER

K-Number: K844768 · 1985-01-25

ApplicantAbbott Laboratories
Decision Date1985-01-25
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ABBOTT LIFECARE 500 INFUSER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1985-01-25 under 510(k) number K844768. 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 ABBOTT LIFECARE 500 INFUSER?

ABBOTT LIFECARE 500 INFUSER is a medical device that received FDA 510(k) clearance on 1985-01-25. The listed applicant is Abbott Laboratories. The 510(k) number is K844768.

When did ABBOTT LIFECARE 500 INFUSER receive FDA 510(k) clearance?

ABBOTT LIFECARE 500 INFUSER received FDA 510(k) clearance on 1985-01-25, under 510(k) number K844768.

Who is the listed applicant for ABBOTT LIFECARE 500 INFUSER?

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 ABBOTT LIFECARE 500 INFUSER?

The FDA product code for ABBOTT LIFECARE 500 INFUSER 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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