510(k) K934895
K934895 is an FDA 510(k) premarket notification submitted by Axiom Medical, Inc. for the device "GLASSMAN SILICONE CATHETER". The FDA issued a decision of Substantially Equivalent on October 13, 1994. The device falls under product code EZL (Catheter, Retention Type, Balloon), a Class II device regulated under 21 CFR 876.5130. Axiom Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 13, 1994
- Date Received
- October 5, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Retention Type, Balloon
- Device Class
- Class II
- Regulation Number
- 876.5130
- Review Panel
- GU
- Submission Type