510(k) K760068
K760068 is an FDA 510(k) premarket notification submitted by New England Nuclear for the device "KIT, RIA, GENTAMICIN SULF.". The FDA issued a decision of Substantially Equivalent on July 20, 1976. The device falls under product code DJB (Radioimmunoassay, Gentamicin (125-I), Second Antibody Sep.), a Class II device regulated under 21 CFR 862.3450. New England Nuclear has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 20, 1976
- Date Received
- June 16, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Gentamicin (125-I), Second Antibody Sep.
- Device Class
- Class II
- Regulation Number
- 862.3450
- Review Panel
- TX
- Submission Type