510(k) K974759
K974759 is an FDA 510(k) premarket notification submitted by Hydrox Laboratories for the device "HYDROX SALINE SOLUTION 0.9% SODIUM CHLORIDE 4 OZ. CUP 120 ML 100 ML BOTTLE". The FDA issued a decision of Substantially Equivalent on March 9, 1998. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Hydrox Laboratories has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 9, 1998
- Date Received
- December 19, 1997
- 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