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FDA 510(k)

LIFECARE MICRO PUMP

K-Number: K832289 · 1983-09-12

ApplicantAbbott Laboratories
Decision Date1983-09-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFECARE MICRO 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 1983-09-12 under 510(k) number K832289. 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 MICRO PUMP?

LIFECARE MICRO PUMP is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Abbott Laboratories. The 510(k) number is K832289.

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

LIFECARE MICRO PUMP received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832289.

Who is the listed applicant for LIFECARE MICRO 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 MICRO PUMP?

The FDA product code for LIFECARE MICRO 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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