510(k) K961242
K961242 is an FDA 510(k) premarket notification submitted by Allergan, Inc. for the device "AMO PHACOFLEX II INTERSECTION SYSTEM". The FDA issued a decision of Substantially Equivalent on June 17, 1996. The device falls under product code KYB (Lens, Guide, Intraocular), a Class I device regulated under 21 CFR 886.4300. Allergan, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 17, 1996
- Date Received
- April 1, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lens, Guide, Intraocular
- Device Class
- Class I
- Regulation Number
- 886.4300
- Review Panel
- OP
- Submission Type