510(k) K861825

CORNEAL TRANSPLANT TREPHINE DISPOSABLE BLADE by Storz Instrument Co. — Product Code HRH

K861825 is an FDA 510(k) premarket notification submitted by Storz Instrument Co. for the device "CORNEAL TRANSPLANT TREPHINE DISPOSABLE BLADE". The FDA issued a decision of Substantially Equivalent on June 9, 1986. The device falls under product code HRH (Trephine, Manual, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Storz Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 9, 1986
Date Received
May 12, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Trephine, Manual, Ophthalmic
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type