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FDA 510(k)

MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6

K-Number: K981125 · 1999-02-26

ApplicantMedical Components, Inc.
Decision Date1999-02-26
Product CodeMSD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1999-02-26 under 510(k) number K981125. 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 MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6?

MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6 is a medical device that received FDA 510(k) clearance on 1999-02-26. The listed applicant is Medical Components, Inc.. The 510(k) number is K981125.

When did MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6 receive FDA 510(k) clearance?

MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6 received FDA 510(k) clearance on 1999-02-26, under 510(k) number K981125.

Who is the listed applicant for MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6?

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

What is the FDA product code for MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6?

The FDA product code for MEDCOMP TESIO CATHETER, MODELS MBR-6, MBL-6, MBS-6 is MSD.

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Related Devices (Code: MSD)

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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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