510(k) K974295
K974295 is an FDA 510(k) premarket notification submitted by Byron Medical for the device "BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING". The FDA issued a decision of Substantially Equivalent on February 10, 1998. The device falls under product code KGZ (Accessories, Catheter), a Class I device regulated under 21 CFR 878.4200. Byron Medical has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 10, 1998
- Date Received
- November 14, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accessories, Catheter
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type