510(k) K770256

CATHETERS, SILICONE COATED by Pharmaseal Div., Baxter Healthcare Corp. — Product Code KOD

K770256 is an FDA 510(k) premarket notification submitted by Pharmaseal Div., Baxter Healthcare Corp. for the device "CATHETERS, SILICONE COATED". The FDA issued a decision of Substantially Equivalent on February 17, 1977. The device falls under product code KOD (Catheter, Urological), a Class II device regulated under 21 CFR 876.5130. Pharmaseal Div., Baxter Healthcare Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 17, 1977
Date Received
February 10, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Urological
Device Class
Class II
Regulation Number
876.5130
Review Panel
GU
Submission Type