510(k) K760763
K760763 is an FDA 510(k) premarket notification submitted by Dynatech Cryomedical Co. for the device "COLPOSCOPE (DYNATECH COLPOSCOPE-MODEL I". The FDA issued a decision of Substantially Equivalent on October 20, 1976. The device falls under product code HEX (Colposcope (And Colpomicroscope)), a Class II device regulated under 21 CFR 884.1630. Dynatech Cryomedical Co. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 20, 1976
- Date Received
- October 4, 1976
- 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