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FDA 510(k)

ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS

K-Number: K970864 · 1997-10-17

ApplicantArrow Intl., Inc.
Decision Date1997-10-17
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS 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 1997-10-17 under 510(k) number K970864. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS?

ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS is a medical device that received FDA 510(k) clearance on 1997-10-17. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K970864.

When did ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS receive FDA 510(k) clearance?

ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS received FDA 510(k) clearance on 1997-10-17, under 510(k) number K970864.

Who is the listed applicant for ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS 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 ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS?

The FDA product code for ARROW-HOWES LARGE BORE MULTI-LUMEN CENTRAL VENOUS CATHETERS is FOZ.

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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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