510(k) K974295

BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING by Byron Medical — Product Code KGZ

K974295 is an FDA 510(k) premarket notification submitted by Byron Medical for the device "BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING". The FDA issued a decision of Substantially Equivalent on February 10, 1998. The device falls under product code KGZ (Accessories, Catheter), a Class I device regulated under 21 CFR 878.4200. Byron Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 10, 1998
Date Received
November 14, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, Catheter
Device Class
Class I
Regulation Number
878.4200
Review Panel
SU
Submission Type