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FDA 510(k)

LAKE CATHETER CARE KITS (MODIFICATION)

K-Number: K875383 · 1988-03-09

ApplicantLake Medical Products, Inc.
Decision Date1988-03-09
Product CodeKOD
Advisory CommitteeGU
DecisionUnknown

Device Summary

LAKE CATHETER CARE KITS (MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Lake Medical Products, Inc.. It received FDA 510(k) clearance on 1988-03-09 under 510(k) number K875383. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LAKE CATHETER CARE KITS (MODIFICATION)?

LAKE CATHETER CARE KITS (MODIFICATION) is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is Lake Medical Products, Inc.. The 510(k) number is K875383.

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

LAKE CATHETER CARE KITS (MODIFICATION) received FDA 510(k) clearance on 1988-03-09, under 510(k) number K875383.

Who is the listed applicant for LAKE CATHETER CARE KITS (MODIFICATION)?

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

What is the FDA product code for LAKE CATHETER CARE KITS (MODIFICATION)?

The FDA product code for LAKE CATHETER CARE KITS (MODIFICATION) is KOD.

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Other records listing Lake Medical Products, 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.

K943162LAKE STAGEZERO(TM) AIR FLOTATION BEDK922730LAKE OSTOMY CARE SETK905053STAGE ZERO AIR FLOTATION BEDK901835LAKE N/G FEEDING TUBE (WITH Y PORT CONNECTOR)K902508LAKE MALE EXTERNAL CATHETERIZATION KITK902121LAKE GASTROSTOMY TUBE

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Related Devices (Code: KOD)

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.

K251864Rubber Utility CatheterC.R. Bard, Inc.K220036Wellead Ureteral CatheterWell Lead Medical Co., Ltd.K220730allFlex Ureteral Catheters, Krait Ureteral CathetersAllwin Medical Devices, Inc.K211032Urinary Catheter 12 Fr, Urinary Catheter 16 FrUrogen Pharma, Ltd.K181979Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent CatheterTeleflexmedical, Inc.K180354UroGen Ureteral CatheterUrogen Pharma, Ltd.

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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