510(k) K912717
K912717 is an FDA 510(k) premarket notification submitted by J.S. Medical Assoc. for the device "J&S UIBC REAGENTS". The FDA issued a decision of Substantially Equivalent on September 25, 1991. The device falls under product code JMO (Ferrozine (Colorimetric) Iron Binding Capacity), a Class I device regulated under 21 CFR 862.1415. J.S. Medical Assoc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 25, 1991
- Date Received
- June 18, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ferrozine (Colorimetric) Iron Binding Capacity
- Device Class
- Class I
- Regulation Number
- 862.1415
- Review Panel
- CH
- Submission Type