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FDA 510(k)

CATHETER CARE KITS

K-Number: K894611 · 1989-12-15

ApplicantL H M Ent., Inc.
Decision Date1989-12-15
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

CATHETER CARE KITS is the device name listed in this FDA 510(k) record. The listed applicant is L H M Ent., Inc.. It received FDA 510(k) clearance on 1989-12-15 under 510(k) number K894611. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CATHETER CARE KITS?

CATHETER CARE KITS is a medical device that received FDA 510(k) clearance on 1989-12-15. The listed applicant is L H M Ent., Inc.. The 510(k) number is K894611.

When did CATHETER CARE KITS receive FDA 510(k) clearance?

CATHETER CARE KITS received FDA 510(k) clearance on 1989-12-15, under 510(k) number K894611.

Who is the listed applicant for CATHETER CARE KITS?

The FDA 510(k) record lists L H M Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER CARE KITS?

The FDA product code for CATHETER CARE KITS is FOZ.

Related Clinical Trials

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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Other records listing L H M Ent., 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.

K901078SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN 0.9% SALINEK901079SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN STER. WATERK894610CUSTOM TRAYS, KITSK900439SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CCK883506IRRIGATION KIT

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

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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