510(k) K945172

VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS by Visitec Co. — Product Code HQX

K945172 is an FDA 510(k) premarket notification submitted by Visitec Co. for the device "VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS". The FDA issued a decision of Substantially Equivalent on January 17, 1995. The device falls under product code HQX (Implant, Orbital, Extra-Ocular), a Class II device regulated under 21 CFR 886.3340. Visitec Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 17, 1995
Date Received
October 21, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Implant, Orbital, Extra-Ocular
Device Class
Class II
Regulation Number
886.3340
Review Panel
OP
Submission Type