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FDA 510(k)

CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER

K-Number: K884552 · 1989-03-14

ApplicantArrow Intl., Inc.
Decision Date1989-03-14
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1989-03-14 under 510(k) number K884552. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER?

CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER is a medical device that received FDA 510(k) clearance on 1989-03-14. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K884552.

When did CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER receive FDA 510(k) clearance?

CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER received FDA 510(k) clearance on 1989-03-14, under 510(k) number K884552.

Who is the listed applicant for CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER?

The FDA 510(k) record lists Arrow Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER?

The FDA product code for CONTINUOUS EPIDURAL ANESTHESIA KIT W/POLY CATHETER is CAZ.

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Related Devices (Code: CAZ)

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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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