510(k) K883352
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 6, 1988
- Date Received
- August 9, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antiserum, Fluorescent, Chlamydia Trachomatis
- Device Class
- Class I
- Regulation Number
- 866.3120
- Review Panel
- MI
- Submission Type