510(k) K182764
K182764 is an FDA 510(k) premarket notification submitted by Biop Medical , Ltd. for the device "Biop Digital Colposcope". The FDA issued a decision of Substantially Equivalent on November 27, 2018. The device falls under product code HEX (Colposcope (And Colpomicroscope)), a Class II device regulated under 21 CFR 884.1630.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 27, 2018
- Date Received
- September 28, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Colposcope (And Colpomicroscope)
- Device Class
- Class II
- Regulation Number
- 884.1630
- Review Panel
- OB
- Submission Type