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FDA 510(k)

RESUBMITTED ABBOTT LIFECARE MODEL 3 HB PUMP

K-Number: K890282 · 1989-04-19

ApplicantAbbott Laboratories
Decision Date1989-04-19
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RESUBMITTED ABBOTT LIFECARE MODEL 3 HB 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 1989-04-19 under 510(k) number K890282. 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 RESUBMITTED ABBOTT LIFECARE MODEL 3 HB PUMP?

RESUBMITTED ABBOTT LIFECARE MODEL 3 HB PUMP is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is Abbott Laboratories. The 510(k) number is K890282.

When did RESUBMITTED ABBOTT LIFECARE MODEL 3 HB PUMP receive FDA 510(k) clearance?

RESUBMITTED ABBOTT LIFECARE MODEL 3 HB PUMP received FDA 510(k) clearance on 1989-04-19, under 510(k) number K890282.

Who is the listed applicant for RESUBMITTED ABBOTT LIFECARE MODEL 3 HB 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 RESUBMITTED ABBOTT LIFECARE MODEL 3 HB PUMP?

The FDA product code for RESUBMITTED ABBOTT LIFECARE MODEL 3 HB 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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