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FDA 510(k)

CONTINUOUS EPIDURAL ANESTH. KITS W/NYLON CATHETERS

K-Number: K873943 · 1987-10-20

ApplicantArrow Intl., Inc.
Decision Date1987-10-20
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS EPIDURAL ANESTH. KITS W/NYLON CATHETERS 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 1987-10-20 under 510(k) number K873943. 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 ANESTH. KITS W/NYLON CATHETERS?

CONTINUOUS EPIDURAL ANESTH. KITS W/NYLON CATHETERS is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K873943.

When did CONTINUOUS EPIDURAL ANESTH. KITS W/NYLON CATHETERS receive FDA 510(k) clearance?

CONTINUOUS EPIDURAL ANESTH. KITS W/NYLON CATHETERS received FDA 510(k) clearance on 1987-10-20, under 510(k) number K873943.

Who is the listed applicant for CONTINUOUS EPIDURAL ANESTH. KITS W/NYLON CATHETERS?

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 ANESTH. KITS W/NYLON CATHETERS?

The FDA product code for CONTINUOUS EPIDURAL ANESTH. KITS W/NYLON CATHETERS 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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