Tum-E-Vac Bite Block

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K921946 ↗

FDA Product Code

JXL

Device Class

Class II

Regulation

21 CFR Part 882.5070

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Ethox Neonatal Blood Pressure Cuff-Sterile/Dispos.

  Class II

  FDA 510(k) K844988 Active Cleared 4 Apr 1985

• Weighted Feeding Tube W/Pre-Inserted

  Class II

  FDA 510(k) K841014 Active Cleared 1 May 1984

• Tum-E-Vac

  Class II

  FDA 510(k) K962850 Active Cleared 21 Feb 1997

• Ethox Weighted Feeding Tube

  Class II

  FDA 510(k) K834554 Active Cleared 10 Feb 1984

• Ethox Lavage Tube

  Class II

  FDA 510(k) K860599 Active Cleared 11 Mar 1986

• Surgi-Kit

  Class II

  FDA 510(k) K770590 Active Cleared 14 Apr 1977

See all devices from Ethox Corp. →