510(k) K874241

OPMI MD SURGICAL MICROSCOPE by Carl Zeiss, Inc. — Product Code FSO

K874241 is an FDA 510(k) premarket notification submitted by Carl Zeiss, Inc. for the device "OPMI MD SURGICAL MICROSCOPE". The FDA issued a decision of Substantially Equivalent on December 23, 1987. The device falls under product code FSO (Microscope, Surgical, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4700. Carl Zeiss, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 23, 1987
Date Received
October 15, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Microscope, Surgical, General & Plastic Surgery
Device Class
Class I
Regulation Number
878.4700
Review Panel
SU
Submission Type