510(k) K820460
K820460 is an FDA 510(k) premarket notification submitted by Superior Plastic Products Corp. for the device "3.5 & 5.5 OZ. SODIUM CHLORIDE SOLUTION". The FDA issued a decision of Substantially Equivalent on March 8, 1982. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Superior Plastic Products Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 8, 1982
- Date Received
- February 19, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter And Tip, Suction
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type