510(k) K760074
K760074 is an FDA 510(k) premarket notification submitted by J.T. Baker Chemical Co. for the device "KIT, MORPHINE (TOXI-PAK IMMUNO HI)". The FDA issued a decision of Substantially Equivalent on July 20, 1976. The device falls under product code DLR (Hemagglutination Inhibition, Morphine), a Class II device regulated under 21 CFR 862.3640. J.T. Baker Chemical Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 20, 1976
- Date Received
- June 18, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Hemagglutination Inhibition, Morphine
- Device Class
- Class II
- Regulation Number
- 862.3640
- Review Panel
- TX
- Submission Type