510(k) K950318

FLEX BLUE by King Systems Corp. — Product Code CBH

K950318 is an FDA 510(k) premarket notification submitted by King Systems Corp. for the device "FLEX BLUE". The FDA issued a decision of Substantially Equivalent on February 13, 1995. The device falls under product code CBH (Device, Fixation, Tracheal Tube), a Class I device regulated under 21 CFR 868.5770. King Systems Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 13, 1995
Date Received
January 26, 1995
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