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FDA 510(k)

MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS

K-Number: K981365 · 1998-11-25

ApplicantSherwood Medical Co.
Decision Date1998-11-25
Product CodeMSD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1998-11-25 under 510(k) number K981365. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS?

MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS is a medical device that received FDA 510(k) clearance on 1998-11-25. The listed applicant is Sherwood Medical Co.. The 510(k) number is K981365.

When did MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS receive FDA 510(k) clearance?

MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS received FDA 510(k) clearance on 1998-11-25, under 510(k) number K981365.

Who is the listed applicant for MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS?

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

What is the FDA product code for MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS?

The FDA product code for MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS is MSD.

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Related Devices (Code: MSD)

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.

K241581Hemodialysis CatheterHaolang Medical USA CorporationK210461End CapMedical Components Inc (Medcomp)K203575GlidePath Retro Long-Term Hemodialysis CatheterC.R. Bard, Inc.K211410GlidePath 13F Long-Term Hemodialysis CatheterBard Peripheral Vascular, Inc.K203767Pristine Long-Term Hemodialysis CatheterC B Bard, Inc.K202150GlidePath 7.5F Long-Term Dialysis CatheterC.R. Bard, Inc.

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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