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FDA 510(k)

MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR

K-Number: K000087 · 2000-03-17

ApplicantThe Kendal Co.
Decision Date2000-03-17
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 2000-03-17 under 510(k) number K000087. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR?

MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR is a medical device that received FDA 510(k) clearance on 2000-03-17. The listed applicant is The Kendal Co.. The 510(k) number is K000087.

When did MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR receive FDA 510(k) clearance?

MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR received FDA 510(k) clearance on 2000-03-17, under 510(k) number K000087.

Who is the listed applicant for MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR?

The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR?

The FDA product code for MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR is FOZ.

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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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