MTP Clearvision Disposable Tubing Set

FDA 510(k) K020599 · Mtp Medical Technical Promotion GmbH

Substantially Equivalent

510(k) numberK020599

Submission

Device name
MTP Clearvision Disposable Tubing Set
Applicant
Mtp Medical Technical Promotion GmbH
Culver City, CA, US
Received
February 22, 2002
Decision date
March 13, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EOB – Nasopharyngoscope (Flexible Or Rigid)
Device class
Class II (moderate risk)
Regulation
21 CFR 874.4760
Specialty
Ear, Nose, Throat

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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More from Atmos Medizintechnik GmbH & Co. KG

510(k)DeviceDecision
K091178MTP Disposable Equipment Covers, Karl Storz 15 Touch ScreenMMP · Traditional 07/31/2009SE
K021811Unidrive II Plus Disposable Tubing SetERL · Traditional 06/19/2002SE
K011360MTP Laparomat Disposable Tubing SetGCJ · Traditional 07/19/2001SE
K000337MTP Disposable Trocar ValvesGCJ · Traditional 04/12/2000SE
K994066MTP Disposable TrocarsGCJ · Traditional 01/20/2000SE
K990912MTP Extraction BagGCJ · Traditional 06/09/1999SE
K990909MTP Uropump Disposable Tubing SetLJH · Traditional 06/09/1999SE
K990911MTP Arthropump Disposable Tubing SetHRX · Traditional 06/03/1999SE
K990910MTP Hamou Endomat Disposable Tubing SetsHIH · Traditional 06/03/1999SE

Questions and answers

When was MTP Clearvision Disposable Tubing Set cleared by the FDA?

MTP Clearvision Disposable Tubing Set (K020599) received a 510(k) decision of Substantially Equivalent on March 13, 2002, 19 days after the submission was received.

What is the product code of K020599?

The FDA product code is EOB – Nasopharyngoscope (Flexible Or Rigid), a Class II (moderate risk) device regulated under 21 CFR 874.4760.