510(k) K904366
K904366 is an FDA 510(k) premarket notification submitted by Douglas James Donaldson Compliance Services for the device "CRYSTAL FOCUS EMERALD-CW LASER PHOTOCOAGULATOR". The FDA issued a decision of Substantially Equivalent on October 19, 1990. The device falls under product code HQF (Laser, Ophthalmic), a Class II device regulated under 21 CFR 886.4390. Douglas James Donaldson Compliance Services has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 19, 1990
- Date Received
- September 24, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Laser, Ophthalmic
- Device Class
- Class II
- Regulation Number
- 886.4390
- Review Panel
- OP
- Submission Type