510(k) K952345
K952345 is an FDA 510(k) premarket notification submitted by Medi-Tech, Inc. for the device "MEDI-TECH PLATFORM GUIDE CATHETER". The FDA issued a decision of Substantially Equivalent on August 17, 1995. The device falls under product code DQY (Catheter, Percutaneous), a Class II device regulated under 21 CFR 870.1250. Medi-Tech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 17, 1995
- Date Received
- May 19, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Percutaneous
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- CV
- Submission Type