510(k) K852150

CLINICAL WIDEFIELD SPECULAR MICRISCOPE 500 by Keeler Instruments, Inc. — Product Code HRM

K852150 is an FDA 510(k) premarket notification submitted by Keeler Instruments, Inc. for the device "CLINICAL WIDEFIELD SPECULAR MICRISCOPE 500". The FDA issued a decision of Substantially Equivalent on June 3, 1985. The device falls under product code HRM (Microscope, Operating & Accessories, Ac-Powered, Ophthalmic), a Class I device regulated under 21 CFR 878.4700. Keeler Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 1985
Date Received
May 17, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Microscope, Operating & Accessories, Ac-Powered, Ophthalmic
Device Class
Class I
Regulation Number
878.4700
Review Panel
SU
Submission Type