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FDA 510(k)

TRIP TONOMETRY CATHETER, 8F

K-Number: K992181 · 1999-08-24

ApplicantDatex-Ohmeda, Inc.
Decision Date1999-08-24
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRIP TONOMETRY CATHETER, 8F is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda, Inc.. It received FDA 510(k) clearance on 1999-08-24 under 510(k) number K992181. 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 TRIP TONOMETRY CATHETER, 8F?

TRIP TONOMETRY CATHETER, 8F is a medical device that received FDA 510(k) clearance on 1999-08-24. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K992181.

When did TRIP TONOMETRY CATHETER, 8F receive FDA 510(k) clearance?

TRIP TONOMETRY CATHETER, 8F received FDA 510(k) clearance on 1999-08-24, under 510(k) number K992181.

Who is the listed applicant for TRIP TONOMETRY CATHETER, 8F?

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

What is the FDA product code for TRIP TONOMETRY CATHETER, 8F?

The FDA product code for TRIP TONOMETRY CATHETER, 8F is 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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