510(k) K860088

PL EXAM LIGHT by Burton Medical Products Corp. — Product Code FTD

K860088 is an FDA 510(k) premarket notification submitted by Burton Medical Products Corp. for the device "PL EXAM LIGHT". The FDA issued a decision of Substantially Equivalent on January 24, 1986. The device falls under product code FTD (Lamp, Surgical), a Class II device regulated under 21 CFR 878.4580. Burton Medical Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1986
Date Received
January 10, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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