510(k) K972840
K972840 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "N ANTISERUM TO HUMAN TRANSFERRIN". The FDA issued a decision of Substantially Equivalent on October 17, 1997. The device falls under product code DDG (Transferrin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5880. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 17, 1997
- Date Received
- August 1, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transferrin, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5880
- Review Panel
- IM
- Submission Type