510(k) K910996

OPTI-PLAST 5F PTA CATHETERS by Vas-Cath, Inc. — Product Code LIT

K910996 is an FDA 510(k) premarket notification submitted by Vas-Cath, Inc. for the device "OPTI-PLAST 5F PTA CATHETERS". The FDA issued a decision of Substantially Equivalent on April 9, 1991. The device falls under product code LIT (Catheter, Angioplasty, Peripheral, Transluminal), a Class II device regulated under 21 CFR 870.1250. Vas-Cath, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 9, 1991
Date Received
March 4, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Angioplasty, Peripheral, Transluminal
Device Class
Class II
Regulation Number
870.1250
Review Panel
CV
Submission Type