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

F1 DIODE LASER SYSTEM

K Number: K030235 · Decision Apr 23, 2003
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
13
Review Days
90

Basic Information

Device Name
F1 DIODE LASER SYSTEM
K Number
K030235
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
OPUS MEDICAL, INC.
Date Received
January 23, 2003
Decision Date
April 23, 2003
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

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K033317 SMARTSTITCH M-CONNECTOR, MODEL OM-8700; NEEDLE CASSETTE, OM-8750; AUTOCUFF SYSTEM INSTRUMENT SET, OM-9070
K030170 REUSABLE SMARTSTITCH SUTURE DEVICE, MODELS OM-8007, OM-8500
K031083 OPUS MAGNUM IMPLANT SYSTEM, MODEL OM-1500
K023843 SMARTSTITCH M-CONNECTOR, MODEL OM-8005; SMARTSTITCH ACTUATION HANDLE, MODEL OM-8500; AND SMARTSTITCH SUTURE CARTRIDGE
K022229 SMARTSTITCH SUTURE DEVICE, MODEL OM-8500
K020172 OPUS MAGNUM ANCHOR & INSTRUMENT SET
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