510(k) K013938
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 28, 2002
- Date Received
- November 28, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Acid, Lactic, Enzymatic Method
- Device Class
- Class I
- Regulation Number
- 862.1450
- Review Panel
- CH
- Submission Type