510(k) K922273
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 19, 1992
- Date Received
- May 14, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Nephelometer, For Clinical Use
- Device Class
- Class I
- Regulation Number
- 862.2700
- Review Panel
- CH
- Submission Type