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FDA 510(k)

LIFECARE I.V. PUMP - MODEL III

K-Number: K772094 · 1977-12-08

ApplicantAbbott Laboratories
Decision Date1977-12-08
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFECARE I.V. PUMP - MODEL III is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1977-12-08 under 510(k) number K772094. 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 I.V. PUMP - MODEL III?

LIFECARE I.V. PUMP - MODEL III is a medical device that received FDA 510(k) clearance on 1977-12-08. The listed applicant is Abbott Laboratories. The 510(k) number is K772094.

When did LIFECARE I.V. PUMP - MODEL III receive FDA 510(k) clearance?

LIFECARE I.V. PUMP - MODEL III received FDA 510(k) clearance on 1977-12-08, under 510(k) number K772094.

Who is the listed applicant for LIFECARE I.V. PUMP - MODEL III?

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 I.V. PUMP - MODEL III?

The FDA product code for LIFECARE I.V. PUMP - MODEL III 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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