510(k) K962217
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 27, 1996
- Date Received
- June 10, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dna Probe, Nucleic Acid Amplification, Chlamydia
- Device Class
- Class I
- Regulation Number
- 866.3120
- Review Panel
- MI
- Submission Type