510(k) K905422

PVC ROUND WOUND DRAINS by Axiom Medical, Inc. — Product Code GBX

K905422 is an FDA 510(k) premarket notification submitted by Axiom Medical, Inc. for the device "PVC ROUND WOUND DRAINS". The FDA issued a decision of Substantially Equivalent on February 11, 1991. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. Axiom Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 11, 1991
Date Received
December 4, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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