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Stabiltrach

by B&B Medical Technologies, Inc.

510(k) K935171

Stabiltrach is a medical device (FDA Class I; FDA product code CBH, Device, Fixation, Tracheal Tube) made by B&B Medical Technologies, Inc., cleared under FDA 510(k) K935171 on 2 Dec 1993, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK935171 Date2 Dec 1993ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
CBH
Device class
Class I
Regulation
21 CFR Part 868.5770
Advisory committee
Anesthesiology
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code CBH (Device, Fixation, Tracheal Tube).

Other devices from B & B Medical Technologies, Inc.

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