510(k) K873385

OPHTHALMIC PHACO-BLADE by Myocure, Inc. — Product Code HNN

K873385 is an FDA 510(k) premarket notification submitted by Myocure, Inc. for the device "OPHTHALMIC PHACO-BLADE". The FDA issued a decision of Substantially Equivalent on September 21, 1987. The device falls under product code HNN (Knife, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Myocure, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 21, 1987
Date Received
August 24, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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