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FDA 510(k)

ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE

K-Number: K862153 · 1986-12-11

ApplicantArrow Intl., Inc.
Decision Date1986-12-11
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE 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 1986-12-11 under 510(k) number K862153. 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 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE?

ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE is a medical device that received FDA 510(k) clearance on 1986-12-11. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K862153.

When did ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE receive FDA 510(k) clearance?

ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE received FDA 510(k) clearance on 1986-12-11, under 510(k) number K862153.

Who is the listed applicant for ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE?

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 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE?

The FDA product code for ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE is FOZ.

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: 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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