510(k) K861289

BASIC LIGHT by Burton Medical Products Corp. — Product Code KZF

K861289 is an FDA 510(k) premarket notification submitted by Burton Medical Products Corp. for the device "BASIC LIGHT". The FDA issued a decision of Substantially Equivalent on April 18, 1986. The device falls under product code KZF (Device, Medical Examination, Ac Powered), a Class I device regulated under 21 CFR 880.6320. Burton Medical Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 18, 1986
Date Received
April 7, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Medical Examination, Ac Powered
Device Class
Class I
Regulation Number
880.6320
Review Panel
HO
Submission Type