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FDA 510(k)

BRACHIAL PLEXUS CATHETER - BP-01200

K-Number: K874105 · 1987-11-24

ApplicantArrow Intl., Inc.
Decision Date1987-11-24
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BRACHIAL PLEXUS CATHETER - BP-01200 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 1987-11-24 under 510(k) number K874105. 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 BRACHIAL PLEXUS CATHETER - BP-01200?

BRACHIAL PLEXUS CATHETER - BP-01200 is a medical device that received FDA 510(k) clearance on 1987-11-24. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K874105.

When did BRACHIAL PLEXUS CATHETER - BP-01200 receive FDA 510(k) clearance?

BRACHIAL PLEXUS CATHETER - BP-01200 received FDA 510(k) clearance on 1987-11-24, under 510(k) number K874105.

Who is the listed applicant for BRACHIAL PLEXUS CATHETER - BP-01200?

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 BRACHIAL PLEXUS CATHETER - BP-01200?

The FDA product code for BRACHIAL PLEXUS CATHETER - BP-01200 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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