510(k) K961980
K961980 is an FDA 510(k) premarket notification submitted by Bipore, Inc. for the device "BIPORE BALLOON DILATATION CATHETER". The FDA issued a decision of Substantially Equivalent on September 12, 1996. The device falls under product code LIT (Catheter, Angioplasty, Peripheral, Transluminal), a Class II device regulated under 21 CFR 870.1250. Bipore, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 12, 1996
- Date Received
- May 20, 1996
- 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