510(k) K926495

SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE by Sil-Med Corp. — Product Code GBX

K926495 is an FDA 510(k) premarket notification submitted by Sil-Med Corp. for the device "SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE". The FDA issued a decision of Substantially Equivalent on February 2, 1994. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. Sil-Med Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 2, 1994
Date Received
December 29, 1992
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