(44 days)
Not Found
Not Found
No
The device description details a chemical solution and its manufacturing process, with no mention of software, algorithms, or AI/ML terms.
No.
The device is used to eliminate condensation from lenses and goggles, which are tools used during medical procedures, rather than being applied directly to a patient for therapeutic benefit.
No
This device is an anti-fog solution used to eliminate condensation from optical devices in a sterile surgical setting. Its function is to improve visibility for the user, not to diagnose any medical condition or disease.
No
The device description clearly states it is a "solution" with chemical ingredients, indicating it is a physical product, not software.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is to eliminate condensation from lenses and other devices in the sterile surgical arena. This is a physical function to improve visibility during surgery.
- Device Description: The description details the chemical composition and sterilization process of a solution applied to surfaces.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens derived from the human body (like blood, urine, tissue, etc.) to provide information for diagnosis, monitoring, or treatment.
IVDs are specifically designed to perform tests on biological samples to gain information about a person's health status. Clear-It Anti-Fog Solution does not fit this description.
N/A
Intended Use / Indications for Use
Clear-It Anti-Fog Solution is indicated for use in the sterile surgical arena to eliminate condensation from endoscopic lenses, microscope lenses, goggles and other devices that are likely to fog.
Product codes (comma separated list FDA assigned to the subject device)
OCT
Device Description
Clear-It Anti-Fog is a solution whose primary ingredients are Water, Isopropyl Alcohol, Sodium Alcohol Ether Sulfate, and Ammonium Dodecylbenzene proportionally mixed balanced and packaged according to approved manufacturing processes. Clear-It Anti-Fog is terminally sterilized by gamma irradiation. The appropriate dose was established using ISO 11137 method I protocol. Quarterly dose audits are performed using the same ISO 11137 protocol. Routine production testing prior to release includes pH, cytotoxicity, efficacy, and bacterial endotoxin.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
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Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
sterile surgical arena
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
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Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Not Found
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 876.1500 Endoscope and accessories.
(a)
Identification. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.(b)
Classification —(1)Class II (special controls). The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9.
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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 features a stylized eagle with three curved lines representing its body and wings. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circular pattern around the eagle.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
Preservation Solutions, Inc. John R. Dalpee Regulatory Affairs P. O. Box 937 Elkhorn, WI 53121
JUL 2 7 2015
Re: K022826 Trade/Device Name: Clear-It Anti-Fog Solution Regulation Number: 21 CFR 876.1500 Regulation Name: Endoscope and accessories Regulatory Class: II Product Code: OCT Dated (Date on orig SE ltr): August 19, 2002 Received (Date on orig SE ltr): August 26, 2002
Dear Mr. Dalpee,
This letter corrects our substantially equivalent letter of October 9, 2002.
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
1
Page 2 -
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.
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 Small Manufacturers, International and Consumer Assistance 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 Small Manufacturers, International and Consumer Assistance 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,
Benjamin R. Fisher -S
Benjamin R. Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Image /page/2/Picture/0 description: The image shows the logo for Preservation Solutions, Inc. The logo features the letters "PSI" in a large, bold font. To the right of the letters, the words "Preservation Solutions, Inc." are written in a smaller font, with a line underneath. The logo is simple and professional, and it effectively communicates the company's name.
Ph. (262) 723-6715 Fax (262) 723-4013
P.O. Box 937 Elkhorn, W1 53121-0937
510(k) Number: KO2Z826
Device Name:
Clear-It Anti-Fog Solution
Indications For Use:
Clear-It Anti-Fog Solution is indicated for use in the sterile surgical arena to eliminate condensation from endoscopic lenses, microscope lenses, goggles and other devices that are likely to fog.
Please do not write below this line. Continue on another page if needed
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use 21CFR 801.109
or
Over-The-Counter Use _________________________________________________________________________________________________________________________________________________________
Styt Rivela
(Division Sien-Off) Division of veneral, Restorative and Neuro' gical Devices
510(k) Number K022826
ับบบปป7
3
$\mathcal{P}$$\mathcal{S}$$\mathcal{I}$ Preservation Solutions, Inc.
Ph. (262) 723-6715 F2x (262) 723-4013
P.O. Box 937 Elkhorn, WI 53121-0937
OCT 0 9 2002
510(k) Premarket Notification Information
| Applicant: | Preservation Solutions Inc.
P.O. Box 937
Elkhorn WI. 53121 |
|----------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Device Name | Clear-It® Anti-Fog Solution |
| Registration Number: | Preservation Solutions Inc. Establishment Registration
Number is 2132588 |
| Classification: | Class II, 21 CFR Part 876.1500, Endoscope and/or
Accessories. |
| Product Code: | KOG |
| Panel: | Gastroenterology |
| Device Description: | Clear-It Anti-Fog is a solution whose primary
ingredients are Water, Isopropyl Alcohol, Sodium Alcohol
Ether Sulfate, and Ammonium Dodecylbenzene
proportionally mixed balanced and packaged according to
approved manufacturing processes. Clear-It Anti-Fog is
terminally sterilized by gamma irradiation. The appropriate
dose was established using ISO 11137 method I protocol.
Quarterly dose audits are performed using the same ISO
11137 protocol. Routine production testing prior to release
includes pH, cytotoxicity, efficacy, and bacterial endotoxin. |
| Labeling: | Labeling for this device is contained in Appendix A |
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