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FDA 510(k)

DENT SLEEVE MANOMETRIC CATHETER

K-Number: K881310 · 1988-05-20

ApplicantWilson-Cook Medical, Inc.
Decision Date1988-05-20
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DENT SLEEVE MANOMETRIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K881310. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENT SLEEVE MANOMETRIC CATHETER?

DENT SLEEVE MANOMETRIC CATHETER is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K881310.

When did DENT SLEEVE MANOMETRIC CATHETER receive FDA 510(k) clearance?

DENT SLEEVE MANOMETRIC CATHETER received FDA 510(k) clearance on 1988-05-20, under 510(k) number K881310.

Who is the listed applicant for DENT SLEEVE MANOMETRIC CATHETER?

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

What is the FDA product code for DENT SLEEVE MANOMETRIC CATHETER?

The FDA product code for DENT SLEEVE MANOMETRIC CATHETER is KNT.

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Related Devices (Code: KNT)

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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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