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

ALTUS MEDICAL FAMILY OF COOLGLIDE LASERS, MODELS COOLGLIDE I, COOLGLIDE II, AND FUTURE MODELS

K Number: K022226 · Decision Oct 8, 2002
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
4
Review Days
90

Basic Information

Device Name
ALTUS MEDICAL FAMILY OF COOLGLIDE LASERS, MODELS COOLGLIDE I, COOLGLIDE II, AND FUTURE MODELS
K Number
K022226
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ALTUS MEDICAL, INC.
Date Received
July 10, 2002
Decision Date
October 8, 2002
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

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

View all

Other Clearances by ALTUS MEDICAL, INC.

K Number Device Name
K033768 ALTUS MEDICAL OPTIONAL INFRARED HANDPIECE
K023954 ALTUS MEDICAL COOLGLIDE LASER SYSTEMS AND ACCESSORIES
K014040 FAMILY OF ALTUS MEDICAL MODIFIED COOLGLIDE AESTHETIC LASERS, MODELS COOLGLIDE I, II AND FUTURE MODELS