510(k) K962006
K962006 is an FDA 510(k) premarket notification submitted by Menicon Co, Ltd. for the device "MENICON Z (TISILFOCON A) RIGID GAS PERMEABLE CONTACT LENS". The FDA issued a decision of Substantially Equivalent on October 9, 1996. The device falls under product code HQD (Lens, Contact (Other Material) - Daily), a Class II device regulated under 21 CFR 886.5916. Menicon Co, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 9, 1996
- Date Received
- May 22, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lens, Contact (Other Material) - Daily
- Device Class
- Class II
- Regulation Number
- 886.5916
- Review Panel
- OP
- Submission Type