510(k) K922735

ZIESS ENDOPROBE by Carl Zeiss, Inc. — Product Code HQB

K922735 is an FDA 510(k) premarket notification submitted by Carl Zeiss, Inc. for the device "ZIESS ENDOPROBE". The FDA issued a decision of Substantially Equivalent on July 9, 1992. The device falls under product code HQB (Photocoagulator And Accessories), a Class II device regulated under 21 CFR 886.4690. Carl Zeiss, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 9, 1992
Date Received
June 8, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Photocoagulator And Accessories
Device Class
Class II
Regulation Number
886.4690
Review Panel
OP
Submission Type