510(k) K920064

OPTI-LENS CONTACT LENS CASE by Ryder Intl. Corp. — Product Code LRX

K920064 is an FDA 510(k) premarket notification submitted by Ryder Intl. Corp. for the device "OPTI-LENS CONTACT LENS CASE". The FDA issued a decision of Substantially Equivalent on March 4, 1992. The device falls under product code LRX (Case, Contact Lens), a Class II device regulated under 21 CFR 886.5928. Ryder Intl. Corp. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 4, 1992
Date Received
January 7, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Case, Contact Lens
Device Class
Class II
Regulation Number
886.5928
Review Panel
OP
Submission Type