Ventilation Tube Teflon Shepard Type

FDA 510(k) K781259 · Xomed, Inc.

Substantially Equivalent

510(k) numberK781259

Submission

Device name
Ventilation Tube Teflon Shepard Type
Applicant
Xomed, Inc.
Arnold, MO, US
Received
July 24, 1978
Decision date
August 14, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
ETD – Tube, Tympanostomy
Device class
Class II (moderate risk)
Regulation
21 CFR 874.3880
Specialty
Ear, Nose, Throat
Implant
Yes

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K232702Solo+ Tympanostomy Tube Device (TTD)ETD · Traditional Aventamed Dac05/20/2024SE
K233658Biowy Tym Tube (TT)ETD · Traditional Biowy Corporation02/16/2024SE
K232059Tympanostomy TubesETD · Traditional Grace Medical, Inc.11/24/2023SE
K221254Hummingbird Tympanostomy Tube SystemETD · Traditional Preceptis Medical, Inc.07/27/2022SE
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K171239TULA Tube Delivery SystemETD · Special Tusker Medical06/28/2017SE
K151830Hummingbird Tympanostomy TubeETD · Traditional Preceptis Medical09/21/2015SE
K151067Ventilation (Tympanostomy) TubesETD · Traditional Medtronic Xomed, Inc.07/22/2015SE

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K002897Titanium Middle Ear ProsthesesETB · Traditional 10/11/2000SE
K993653Micro-France Trocars and AccessoriesHET · Traditional 06/09/2000SE
K001148Merogel Otologic PackKHJ · Traditional 06/03/2000SE
K994262Frontal Sinus Trephination CannulaKAM · Traditional 02/08/2000SE
K992855XPS Straightshot or Model 2000 Microdebrider System or XPS PowersculptQPB · Traditional 01/21/2000SE
K993582Modification to Laser-Shield IIBTR · Traditional 01/20/2000SE
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Questions and answers

When was Ventilation Tube Teflon Shepard Type cleared by the FDA?

Ventilation Tube Teflon Shepard Type (K781259) received a 510(k) decision of Substantially Equivalent on August 14, 1978, 21 days after the submission was received.

What is the product code of K781259?

The FDA product code is ETD – Tube, Tympanostomy, a Class II (moderate risk) device regulated under 21 CFR 874.3880.