510(k) K922544

MEDICAM 900 AUTOELECTRONIC LIGHT SOURCE by Kirschner Medical Corp. — Product Code FST

K922544 is an FDA 510(k) premarket notification submitted by Kirschner Medical Corp. for the device "MEDICAM 900 AUTOELECTRONIC LIGHT SOURCE". The FDA issued a decision of Substantially Equivalent on August 7, 1992. The device falls under product code FST (Light, Surgical, Fiberoptic), a Class II device regulated under 21 CFR 878.4580. Kirschner Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 1992
Date Received
May 29, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Light, Surgical, Fiberoptic
Device Class
Class II
Regulation Number
878.4580
Review Panel
SU
Submission Type