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FDA 510(k)

LIFECARE 75 CONTROLLER

K-Number: K893487 · 1989-07-28

ApplicantAbbott Laboratories
Decision Date1989-07-28
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFECARE 75 CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1989-07-28 under 510(k) number K893487. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFECARE 75 CONTROLLER?

LIFECARE 75 CONTROLLER is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Abbott Laboratories. The 510(k) number is K893487.

When did LIFECARE 75 CONTROLLER receive FDA 510(k) clearance?

LIFECARE 75 CONTROLLER received FDA 510(k) clearance on 1989-07-28, under 510(k) number K893487.

Who is the listed applicant for LIFECARE 75 CONTROLLER?

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 75 CONTROLLER?

The FDA product code for LIFECARE 75 CONTROLLER is LDR.

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Related Devices (Code: LDR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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