510(k) K844323

KONAN CLINIC MICROSCOPE CLM-100-150 by Keeler Instruments, Inc. — Product Code HRM

K844323 is an FDA 510(k) premarket notification submitted by Keeler Instruments, Inc. for the device "KONAN CLINIC MICROSCOPE CLM-100-150". The FDA issued a decision of Substantially Equivalent on November 21, 1984. 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
November 21, 1984
Date Received
November 7, 1984
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