510(k) K854507

STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS by Storz Instrument Co. — Product Code LXP

K854507 is an FDA 510(k) premarket notification submitted by Storz Instrument Co. for the device "STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS". The FDA issued a decision of Substantially Equivalent on February 7, 1986. The device falls under product code LXP (Plug, Scleral), a Class II device regulated under 21 CFR 886.4155. Storz Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 7, 1986
Date Received
November 12, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plug, Scleral
Device Class
Class II
Regulation Number
886.4155
Review Panel
OP
Submission Type

Intended to provide temporary closure of a scleral incision during an ophthalmic procedure.