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FDA 510(k)

DUAL LUMEN CATHETER (DLC) TRAY

K-Number: K941851 · 1995-03-13

ApplicantNeostar Medical Technologies, Inc.
Decision Date1995-03-13
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DUAL LUMEN CATHETER (DLC) TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Neostar Medical Technologies, Inc.. It received FDA 510(k) clearance on 1995-03-13 under 510(k) number K941851. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL LUMEN CATHETER (DLC) TRAY?

DUAL LUMEN CATHETER (DLC) TRAY is a medical device that received FDA 510(k) clearance on 1995-03-13. The listed applicant is Neostar Medical Technologies, Inc.. The 510(k) number is K941851.

When did DUAL LUMEN CATHETER (DLC) TRAY receive FDA 510(k) clearance?

DUAL LUMEN CATHETER (DLC) TRAY received FDA 510(k) clearance on 1995-03-13, under 510(k) number K941851.

Who is the listed applicant for DUAL LUMEN CATHETER (DLC) TRAY?

The FDA 510(k) record lists Neostar Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUAL LUMEN CATHETER (DLC) TRAY?

The FDA product code for DUAL LUMEN CATHETER (DLC) TRAY is KOC.

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Other records listing Neostar Medical Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960625SPREADABLE SHEATH INTRODUCER SETK944511ACUTE CENTRAL VENOUS ACCESS CATHETER (ACVAC)K944660ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY

Related Devices (Code: KOC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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