510(k) K942442
K942442 is an FDA 510(k) premarket notification submitted by Acufex Microsurgical, Inc. for the device "ACUFEX T-FIX DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on December 5, 1994. The device falls under product code MIA (Needle, Spinal, Short Term), a Class II device regulated under 21 CFR 868.5150. Acufex Microsurgical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 5, 1994
- Date Received
- May 23, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Spinal, Short Term
- Device Class
- Class II
- Regulation Number
- 868.5150
- Review Panel
- AN
- Submission Type