510(k) K010864
K010864 is an FDA 510(k) premarket notification submitted by Hemagen Diagnostics, Inc. for the device "ANALYST PANELS + ANALYTICAL TEST ROTOR". The FDA issued a decision of Substantially Equivalent on May 21, 2001. The device falls under product code KHS (Enzymatic, Carbon-Dioxide), a Class II device regulated under 21 CFR 862.1160. Hemagen Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 21, 2001
- Date Received
- March 22, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzymatic, Carbon-Dioxide
- Device Class
- Class II
- Regulation Number
- 862.1160
- Review Panel
- CH
- Submission Type