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FDA 510(k)

[CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP

K-Number: K862056 · 1986-08-25

ApplicantArrow Intl., Inc.
Decision Date1986-08-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

[CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP 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 1986-08-25 under 510(k) number K862056. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the [CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP?

[CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP is a medical device that received FDA 510(k) clearance on 1986-08-25. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K862056.

When did [CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP receive FDA 510(k) clearance?

[CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP received FDA 510(k) clearance on 1986-08-25, under 510(k) number K862056.

Who is the listed applicant for [CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP?

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 [CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP?

The FDA product code for [CENTRAL VENOUS][MULTI-LUMEN] CATHETER W/FLEX TIP is DQY.

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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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