510(k) K935171

STABILTRACH by B&B Medical Technologies, Inc. — Product Code CBH

K935171 is an FDA 510(k) premarket notification submitted by B&B Medical Technologies, Inc. for the device "STABILTRACH". The FDA issued a decision of Substantially Equivalent on December 2, 1993. The device falls under product code CBH (Device, Fixation, Tracheal Tube), a Class I device regulated under 21 CFR 868.5770. B&B Medical Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 2, 1993
Date Received
October 26, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Fixation, Tracheal Tube
Device Class
Class I
Regulation Number
868.5770
Review Panel
AN
Submission Type