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FDA 510(k)

STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000

K-Number: K021567 · 2002-06-19

Decision Date2002-06-19
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000 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 2002-06-19 under 510(k) number K021567. 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 STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000?

STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000 is a medical device that received FDA 510(k) clearance on 2002-06-19. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K021567.

When did STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000 receive FDA 510(k) clearance?

STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000 received FDA 510(k) clearance on 2002-06-19, under 510(k) number K021567.

Who is the listed applicant for STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000?

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 STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000?

The FDA product code for STIMUCATH CONTINUOUS NERVE BLOCK SET, PRODUCT NUMBER AB-05000 is CAZ.

Related Clinical Trials

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.

Other records listing Arrow Intl., Inc. as applicant

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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Related Devices (Code: CAZ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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