IRIDEX CycloG6 Laser System, MicroPulse P3 Drive, G-Probe(RFID)
Device Facts
| Record ID | K143154 |
|---|---|
| Device Name | IRIDEX CycloG6 Laser System, MicroPulse P3 Drive, G-Probe(RFID) |
| Applicant | Iridex Corporation |
| Product Code | GEX · General, Plastic Surgery |
| Decision Date | Jan 2, 2015 |
| Decision | SESE |
| Submission Type | Special |
| Regulation | 21 CFR 878.4810 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Indications for Use
The Family of IR.IDEX® IQ Laser Systems (IQ 532 [532nm], IQ 630-670 [630mm-670m], IQ 810 [810nm] [IRIDEX Cyclo G6 Laser System]) and the hand pieces & accessories that are used with them to deliver laser energy in either CW-pulse, MicroPulse TM or LongPulse TM mode. Intended for soft and fibrous tissue, including osseous tissue incision, excision, coagulation, vaporization, ablation and vessel hemostasis in the medical specialties of, dematology, ear, nose and throat (ENT)/ otolaryngology, and ophthalmology as follows: 810nm (IRIDEX Cyclo G6 Laser System) Ophthalmology: The IRIDEX® Cyclo G6 Laser System and Probe Delivery Devices (G-Probe & MicroPulse P3) are used to deliver laser energy in either CW-Pulse (CW) or MicroPulse™ (uP) treatment mode and indicated for the treatment of Glaucoma:
Device Story
The Iridex Cyclo G6 is an 810nm diode laser system used by ophthalmologists in clinical settings to treat glaucoma. The device consists of a main console with a control panel, fiber-optic ports, and an emergency stop; it connects to a footswitch and specialized handpieces (G-Probe or MicroPulse P3). The system delivers laser energy in Continuous Wave (CW) or MicroPulse (uP) modes to perform transscleral cyclophotocoagulation (TSCPC) of the ciliary processes. The physician operates the device via manual or remote controls, adjusting power, interval, and duration settings. The laser energy is delivered to the eye to induce coagulation or ablation of tissue, which helps manage intraocular pressure in patients with open-angle, closed-angle, or refractory glaucoma. The device provides a therapeutic benefit by reducing glaucoma-related pressure through targeted laser delivery.
Clinical Evidence
No clinical data was needed; the device is substantially equivalent to the predicate K071687. Bench testing and software verification/validation were performed.
Technological Characteristics
810nm diode laser; CW, MicroPulse, and LongPulse output modes; ≤5W power; ≤1kHz repetition rate; 630-650nm aiming beam. System includes console, footswitch, and fiber-optic delivery probes. Electrical requirements: 90-130 VAC or 200-240 VAC, 50/60 Hz. Software-controlled parameters for power, interval, and duration.
Indications for Use
Indicated for treatment of glaucoma, including primary open-angle, closed-angle, and refractory glaucoma, via transscleral cyclophotocoagulation of ciliary processes using 810nm laser energy.
Regulatory Classification
Identification
(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.
Predicate Devices
- Family of Iridex IQ Laser Systems (K071687)
Submission Summary (Full Text)
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Image /page/0/Picture/1 description: The image is a black and white logo for the U.S. Department of Health & Human Services. The logo consists of a circular border with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the circumference. Inside the circle is a stylized image of three human profiles facing right, with flowing lines beneath them that resemble fabric or water.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
January 2, 2015
Iridex Corporation c/o Ms. Kathy Maynor Regulatory Consultant 26 Rebecca St. Homosassa, FL 34446
### Re: K143154
Trade/Device Name: Iridex Cyclo G6 (with delivery devices) Regulation Number: 21 CFR 878.4810 Regulation Name: Power Laser Surgical Instruments Regulatory Class: Class II Product Code: GEX Dated: December 4, 2014 Received: December 5, 2014
Dear Ms. Maynor:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
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Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours.
Deborah L. Falls -S
for Malvina B. Eydelman, M.D. Director Division of Ophthalmic and Ear, Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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## Indications for Use
#### 510(k) Number (if known) K143154
### Device Name
Family of IR.IDEX® IQ Laser Systems (IQ 532, IQ 577, IQ 630-670, IQ 810[IRIDEX Cyclo G6 Laser System])
#### Indications for Use (Describe)
The Family of IR.IDEX® IQ Laser Systems (IQ 532 [532nm], IQ 630-670 [630mm-670m], IQ 810 [810nm] [IRIDEX Cyclo G6 Laser System]) and the hand pieces & accessories that are used with them to deliver laser energy in either CW-pulse, MicroPulse TM or LongPulse TM mode. Intended for soft and fibrous tissue, including osseous tissue incision, excision, coagulation, vaporization, ablation and vessel hemostasis in the medical specialties of, dematology, ear, nose and throat (ENT)/ otolaryngology, and ophthalmology as follows:
810nm (IRIDEX Cyclo G6 Laser System)
#### Ophthalmology:
The IRIDEX® Cyclo G6 Laser System and Probe Delivery Devices (G-Probe & MicroPulse P3) are used to deliver laser energy in either CW-Pulse (CW) or MicroPulse™ (uP) treatment mode and indicated for the treatment of Glaucoma:
| | Condition<br>(Indicated for) | Treatment<br>(Intended Use) | CW/μP |
|-------------------------|-------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------|-------|
| MicroPulse P3<br>Device | For the treatment of Glaucoma<br>including:<br>• Primary Open-Angle<br>• Closed-Angle<br>• Refractory | Transscleral<br>cyclophotocoagulation<br>(TSCPC) of the ciliary<br>processes | μP |
| G-Probe | For the treatment of Glaucoma<br>including:<br>• Primary Open-Angle<br>• Closed-Angle<br>• Refractory | Transscleral<br>cyclophotocoagulation<br>(TSCPC) of the ciliary<br>processes | CW |
Type of Use (Select one or both, as applicable)
Prescription Use (Part 21 CFR 801 Subpart D)
O Over-The-Counter Use (21 CFR 801 Subpart C)
#### PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.
#### FOR FDA USE ONLY
Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)
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Section 8 – Special 510(k) Summary
#### I. General Information
Submitter:
Iridex Corporation
Contact Person:
Kathy Maynor
kmaynor77@gmail.com
352-586-3113 (cell)
Summary Preparation Date: October 31, 2014
#### II. Names
Device Name(s): Cyclo G6
Primary Classification Name(s): Electrosurgical cutting and coagulation device and accessories
#### III. Predicate Devices
- K071687 Family of Iridex IQ Laser Systems (IQ 532, IQ 577, IQ 630-670, ● IQ 810)
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#### IV. Product Description
The Iridex Cyclo G6 is comprised of the following main components:
- Main console containing the major electrical components, including:
- Control Panel including control knobs (power, interval, duration or software assigned ● function), treat/standby button, and display;
- Two delivery device fiber-optic connector ports (only one active at a time);
- LIO illumination connection;
- Smart key port for detecting/operating safety filters and/or accessory identification: ●
- Emergency stop switch:
- Key switch; ●
- Connector ports for the footswitch, remote control, and power cord;
- A treatment Footswitch (either wired, wireless, or wireless with PowerAdjust); ●
- A Wired Remote Control that duplicates the control panel; ●
- Delivery Accessories including G-Probeand MicroPulse P3 probe Handpieces. ● Microscope Adapters, and Laser Indirect Ophthalmoscopes (these are not used with the Cyclo G6 but are available for use with the other members of the laser family).
- Optional Cart/Stand ●
#### V. Indications for Use
lndications for Use (same as K071687):
The Family of IRIDEX® IQ Laser Systems (IQ 532 [532nm], IQ 577 [577nm], IQ 630-670 [630nm-670mm]. IO 810 [810nm]) and the hand pieces, delivery devices & accessories that are used with them to deliver laser energy in either CW-pulse, MicroPulse™ or LongPulse TM mode. Intended for soft and fibrous tissue, including osseous tissue incision, excision, coagulation, vaporization, ablation and vessel hemostasis in the medical specialties of, dermatology, ear, nose and throat (ENT)/ otolaryngology, and ophthalmology as follows:
## 532 nm
## Dermatology
- Pigmented Skin Lesions
- Vascular Lesions
## Ear, Nose, and Throat (ENT)/ Otolaryngology
Otosclerotic Hearing loss and/or diseases of the inner ear:
- Stapedectomy
- Stapedotomy
- Myringotomies ●
- Lysis of Adhesions
- Control of Bleeding ●
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- Removal of Acoustic Neuromas
- . Soft tissue Adhesion in Micro/Macro Otologic Procedures
## Ophthalmology
Indicated for retinal photocoagulation, laser trabeculoplasty, iridoplasty including:
- Retinal photocoagulation (RPC) for the treatment of ●
- Diabetic retinopathy, including: o
- Nonproliferative retinopathy .
- Macular edema
- I Proliferative retinopathy
- Retinal tears and detachments о
- Lattice degeneration O
- Age-related macular degeneration (AMD) O
- Retinopathy of prematurity O
- O Sub-retinal (choroidal) neovascularization
- Central and branch retinal vein occlusion O
- Laser trabeculoplasty, iridotomy, iridoplasty for the treatment of glaucoma, including ●
- Primary open angle/Closed angle O
# 577nm
# Dermatology:
- Treatment of Vascular and pigmented lesions
# Ophthalmology:
Indicated for use in photocoagulation of both anterior and posterior segments including:
- Retinal photocoagulation, panretinal photocoagulation and intravitreal . endophotocoagulation of vascular and structural abnormalities of the retina and choroid including :
- proliferative and nonproliferative diabetic retinopathy; о
- choroidal neovascularization; O
- branch retinal vein occlusion; O
- age-related macular degeneration O
- O retinal tears and detachments
- retinopathy of prematurity O
- Iridotomy, iridectomy and trabeculoplasty in angle closure glaucoma and open angle ● glaucoma
## 810nm
## Ophthalmoloqgy:
Indicated for retinal photocoagulation, laser trabeculoplasty, transscleral cyclophotocoagulation, transscleral retinal photocoagulation, iridotomy, including the following examples:
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- Retinal photocoagulation for the treatment of: о
- Diabetic retinopathy, including: O
- Nonproliferative retinopathy .
- . Macular edema
- I Proliferative retinopathy
- Retinal Tears, Detachments and Holes o
- Lattice degeneration O
- Age-related macular degeneration (AMD) with choroidal neovascularization O (CNV)
- Retinopathy of prematurity O
- Sub-retinal (choroidal) neovascularization O
- Central and Branch Retinal Vein Occlusion O
- o Laser trabeculoplasty, Iidotomy, Transscleral Cyclophotocoagulation (TSCPC) for the treatment of glaucoma, including:
-
- Primary open angle o
- O Closed angle
- Refractory Glaucoma (recalcitrant/uncontrolled) O
### No clinical data was needed for these indications. They are identical to those on K071687.
#### VI. Summary of Technological Characteristics
The technological characteristics of the Iridex Cyclo G6 laser are substantially equivalent to those of the predicate device.
| | | K071687 |
|-----------------------------------|------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------|
| Characteristic | Iridex Cyclo G6 | Iridex Family of IQ Lasers |
| Product Code | General & Plastic Surgery | General & Plastic Surgery |
| Regulation | • GEX, 21 CFR 878.4810 | • GEX, 21 CFR 878.4810 |
| Intended Use | Intended for use in dermatology, ear,<br>nose and throat (ENT)/<br>otolaryngology, and ophthalmology | Intended for use in<br>dermatology, ear, nose and<br>throat (ENT)/<br>otolaryngology, and<br>ophthalmology |
| Indications for<br>Use | Exactly the same as K071687 | See K071687 |
| Wavelength | 810nm | 532nm, 577nm, 630-<br>670nm, 810nm |
| | | K071687 |
| Characteristic | Iridex Cyclo G6 | Iridex Family of IQ Lasers |
| Aiming beam | 630nm-650nm | 630nm-650nm |
| Power Watts | ≤ 5W | ≤ 5W |
| Pulse Duration<br>(usec) | 10µsec-60min | 10µsec-60min |
| Output Mode | CW (CW-Pulse, MicroPulse, Long<br>Pulse) | CW (CW-Pulse, MicroPulse,<br>Long Pulse) |
| Repetition rate | ≤ 1kHz | ≤ 1kHz |
| Laser media | Diode, Diode-pumped, frequency<br>doubled, solid state | Diode, Diode-pumped,<br>frequency doubled, solid<br>state |
| User interface | Manual & Remote Controls | Manual & Remote Controls |
| Laser<br>activation | footswitch | footswitch |
| Delivery devices, how<br>supplied | Delivery Devices provided Sterile<br>packaged & non-sterile | Delivery Devices provided<br>Sterile packaged & non-<br>sterile |
| Electrical<br>requirements | 90-130 VAC, 50/60 Hz<br>200-240 VAC, 50/60 Hz | 90-130 VAC, 50/60 Hz<br>200-240 VAC, 50/60 Hz |
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#### VII. Safety and Effectiveness Information
The review of the indications for use and technical characteristics provided demonstrates that the Iridex Cyclo G6 Laser is substantially equivalent to the predicate device and is safe and effective for use for the various indications for use stated.
The software changes that are the subject of this 510(k) were verified and validated in accordance with the Iridex design control procedures.
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# VIII. Conclusion
The Iridex G6 Laser was found to be substantially equivalent to the predicate device.
The Iridex G6 Laser shares identical indications for use, similar design features, and functional features with, and thus are substantially equivalent to, the predicate device.
