510(k) K003638
K003638 is an FDA 510(k) premarket notification submitted by Allergan, Inc. for the device "MOJAVE CATARACT EXTRACTION SYSTEM". The FDA issued a decision of Substantially Equivalent on February 13, 2001. The device falls under product code HQC (Unit, Phacofragmentation), a Class II device regulated under 21 CFR 886.4670. Allergan, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 13, 2001
- Date Received
- November 24, 2000
- Clearance Type
- Abbreviated
- 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