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FDA 510(k)

CONTURA CAVITY MAINTENANCE CATHETER

K-Number: K092323 · 2009-08-19

ApplicantSenorx, Inc.
Decision Date2009-08-19
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONTURA CAVITY MAINTENANCE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Senorx, Inc.. It received FDA 510(k) clearance on 2009-08-19 under 510(k) number K092323. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTURA CAVITY MAINTENANCE CATHETER?

CONTURA CAVITY MAINTENANCE CATHETER is a medical device that received FDA 510(k) clearance on 2009-08-19. The listed applicant is Senorx, Inc.. The 510(k) number is K092323.

When did CONTURA CAVITY MAINTENANCE CATHETER receive FDA 510(k) clearance?

CONTURA CAVITY MAINTENANCE CATHETER received FDA 510(k) clearance on 2009-08-19, under 510(k) number K092323.

Who is the listed applicant for CONTURA CAVITY MAINTENANCE CATHETER?

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

What is the FDA product code for CONTURA CAVITY MAINTENANCE CATHETER?

The FDA product code for CONTURA CAVITY MAINTENANCE CATHETER is JAQ.

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Related Devices (Code: JAQ)

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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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