510(k) K854869

INTRAOCULAR FORCEPS & SCISSORS by Mira, Inc. — Product Code HNR

K854869 is an FDA 510(k) premarket notification submitted by Mira, Inc. for the device "INTRAOCULAR FORCEPS & SCISSORS". The FDA issued a decision of Substantially Equivalent on March 5, 1986. The device falls under product code HNR (Forceps, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Mira, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1986
Date Received
December 4, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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