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FDA 510(k)

LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE

K-Number: K893766 · 1989-11-01

ApplicantAbbott Laboratories
Decision Date1989-11-01
Product CodeMAJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1989-11-01 under 510(k) number K893766. The device is classified under product code MAJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE?

LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE is a medical device that received FDA 510(k) clearance on 1989-11-01. The listed applicant is Abbott Laboratories. The 510(k) number is K893766.

When did LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE receive FDA 510(k) clearance?

LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE received FDA 510(k) clearance on 1989-11-01, under 510(k) number K893766.

Who is the listed applicant for LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE?

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 CONT. EPIDURAL CATH. FOR MORPHINE SULFATE?

The FDA product code for LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATE is MAJ.

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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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