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FDA 510(k)

LIFECARE 175 INFUSER, MODIFICATION

K-Number: K944190 · 1995-05-23

ApplicantAbbott Laboratories
Decision Date1995-05-23
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 1995-05-23 under 510(k) number K944190. 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 1995-05-23. The listed applicant is Abbott Laboratories. The 510(k) number is K944190.

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

LIFECARE 175 INFUSER, MODIFICATION received FDA 510(k) clearance on 1995-05-23, under 510(k) number K944190.

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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