510(k) K951462
K951462 is an FDA 510(k) premarket notification submitted by Allergan Medical Optics for the device "AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM". The FDA issued a decision of Substantially Equivalent on June 15, 1995. The device falls under product code HQC (Unit, Phacofragmentation), a Class II device regulated under 21 CFR 886.4670. Allergan Medical Optics has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 15, 1995
- Date Received
- March 30, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Phacofragmentation
- Device Class
- Class II
- Regulation Number
- 886.4670
- Review Panel
- OP
- Submission Type