FDA 510(k)

A PORT DETACHED CATHETER SYSTEM CATALOG #1002

K-Number: K961583 · 1996-07-18

Decision Date1996-07-18

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

A PORT DETACHED CATHETER SYSTEM CATALOG #1002 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 1996-07-18 under 510(k) number K961583. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A PORT DETACHED CATHETER SYSTEM CATALOG #1002?

A PORT DETACHED CATHETER SYSTEM CATALOG #1002 is a medical device that received FDA 510(k) clearance on 1996-07-18. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K961583.

When did A PORT DETACHED CATHETER SYSTEM CATALOG #1002 receive FDA 510(k) clearance?

A PORT DETACHED CATHETER SYSTEM CATALOG #1002 received FDA 510(k) clearance on 1996-07-18, under 510(k) number K961583.

Who is the listed applicant for A PORT DETACHED CATHETER SYSTEM CATALOG #1002?

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 A PORT DETACHED CATHETER SYSTEM CATALOG #1002?

The FDA product code for A PORT DETACHED CATHETER SYSTEM CATALOG #1002 is LJT.

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Other records listing Arrow Intl., Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.