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FDA 510(k)

19 GA PLASTIC REINFORCED EPIDURAL CATHETER

K-Number: K001587 · 2000-07-12

ApplicantArrow Intl., Inc.
Decision Date2000-07-12
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

19 GA PLASTIC REINFORCED EPIDURAL 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 2000-07-12 under 510(k) number K001587. 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 19 GA PLASTIC REINFORCED EPIDURAL CATHETER?

19 GA PLASTIC REINFORCED EPIDURAL CATHETER is a medical device that received FDA 510(k) clearance on 2000-07-12. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K001587.

When did 19 GA PLASTIC REINFORCED EPIDURAL CATHETER receive FDA 510(k) clearance?

19 GA PLASTIC REINFORCED EPIDURAL CATHETER received FDA 510(k) clearance on 2000-07-12, under 510(k) number K001587.

Who is the listed applicant for 19 GA PLASTIC REINFORCED EPIDURAL 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 19 GA PLASTIC REINFORCED EPIDURAL CATHETER?

The FDA product code for 19 GA PLASTIC REINFORCED EPIDURAL CATHETER is CAZ.

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Other records listing Arrow Intl., Inc. as applicant

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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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