FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LUXTEC ACO SERIES 4000 LIGHT SOURCE

K Number: K890716 · Decision Apr 26, 1989
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
30
Applicant Total
15
Review Days
72

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Basic Information

Device Name
LUXTEC ACO SERIES 4000 LIGHT SOURCE
K Number
K890716
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Luxtec Corp.
Date Received
February 13, 1989
Decision Date
April 26, 1989
Product Code
FCW
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FCW Light Source, Fiberoptic, Routine

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Other Clearances by Luxtec Corp.

K Number Device Name
K973193 LUXSCOPE
K970642 TENOSCOPE
K970562 TENOSNARE
K950960 REDDY ILLUMINATOR
K895248 IMS5000 ILLUMINATED LOUPES
K864387 LUXTEC FIBEROPTIC CABLES
K864383 LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS
K864382 FRAZIER SUCTION TUBE
K864385 LUXTEC LIGHT SOURCES
K864865 SPECULUM, VAGINAL, METAL FIBEROPTIC
Search all 15 clearances from Luxtec Corp. →