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FDA 510(k)

LIFECARE 175 INFUSER -- MODIFICATION

K-Number: K923829 · 1993-04-07

ApplicantAbbott Laboratories
Decision Date1993-04-07
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFECARE 175 INFUSER -- MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1993-04-07 under 510(k) number K923829. 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 175 INFUSER -- MODIFICATION?

LIFECARE 175 INFUSER -- MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Abbott Laboratories. The 510(k) number is K923829.

When did LIFECARE 175 INFUSER -- MODIFICATION receive FDA 510(k) clearance?

LIFECARE 175 INFUSER -- MODIFICATION received FDA 510(k) clearance on 1993-04-07, under 510(k) number K923829.

Who is the listed applicant for LIFECARE 175 INFUSER -- MODIFICATION?

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 175 INFUSER -- MODIFICATION?

The FDA product code for LIFECARE 175 INFUSER -- MODIFICATION 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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