21 C.F.R. · Food and Drugs
21 C.F.R. § 874.3930

Tympanostomy tube with semipermeable membrane.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 874.3930 — Tympanostomy tube with semipermeable membrane.

§ 874.3930 Tympanostomy tube with semipermeable membrane. (a) Identification. A tympanostomy tube with a semipermeable membrane is a device intended to be implanted for ventilation or drainage of the middle ear and for preventing fluids from entering the middle ear cavity. The device is inserted through the tympanic membrane to permit a free exchange of air between the outer ear and middle ear. The tube portion of the device is made of silicone elastomer or porous polyethylene, and the membrane portion is made of polytetrafluoroethylene. (b) Classification. Class II. The special control for this device is FDA's “Tympanostomy Tubes, Submission Guidance for a 510(k).” [51 FR 40389, Nov. 6, 1986, as amended at 65 FR 17145, Mar. 31, 2000]

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21 C.F.R. § 874.3930
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The regulatory text of 21 C.F.R. § 874.3930 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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