510(k) K860695
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 12, 1986
- Date Received
- February 25, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Mycoplasma Detection
- Device Class
- Class I
- Regulation Number
- 864.2360
- Review Panel
- PA
- Submission Type