FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HALUX TASKLIGHT

K Number: K931645 · Decision Aug 20, 1993
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
36
Applicant Total
15
Review Days
140

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HALUX TASKLIGHT
K Number
K931645
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6320
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Burton Medical Products Corp.
Date Received
April 2, 1993
Decision Date
August 20, 1993
Product Code
KZF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KZF Device, Medical Examination, Ac Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KZF), ordered by most recent decision date.

View all

Other Clearances by Burton Medical Products Corp.

K Number Device Name
K101537 AIM 200, MAJOR SURGICAL LIGHT
K042395 OUTPATIENT III MINOR SURGERY LIGHT
K000639 VISIONARY 2000
K963682 GENIE' SINGLE CEILING AND DOUBLE CEILING
K961843 GENIE
K935102 SATURN LIGHT
K942553 GENESIS
K936088 WAVE FLUORESCENT MAGNIFIER
K901706 LIGHT, HEAD, EXAMINATION
K893807 MODEL 0183010, PEARL MEDICAL EXAM LIGHT
Search all 15 clearances from Burton Medical Products Corp. →