(121 days)
No
The device description and performance studies focus on the chemical composition and antimicrobial/cleaning efficacy of a contact lens solution, with no mention of AI or ML.
No.
The device is a contact lens cleaning and disinfecting solution, which is not considered a therapeutic device. Its purpose is to maintain the cleanliness and sterility of contact lenses, not to treat a disease or condition in the human body.
No
Explanation: The device is a multi-purpose disinfecting solution for contact lenses, used for cleaning, protein removal, rinsing, and disinfection. Its intended use is not to diagnose any condition or disease.
No
The device description clearly states it is a sterile, buffered, isotonic, aqueous solution containing various chemical components, indicating it is a physical product (liquid solution) and 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 for cleaning, disinfecting, and storing contact lenses. This is a direct interaction with a medical device (contact lenses) and not a test performed on a biological sample to diagnose a condition or provide information about a physiological state.
- Device Description: The description lists chemical components used for cleaning and disinfection. It does not describe reagents or equipment used for analyzing biological samples.
- Performance Studies: The studies focus on the cleaning and disinfecting efficacy of the solution on contact lenses and its biocompatibility. They do not involve testing biological samples for diagnostic purposes.
- Lack of IVD Indicators: There is no mention of analyzing biological samples, diagnosing conditions, or providing information about a patient's health status based on testing biological materials.
Therefore, OPTI-FREE® EXPRESS® Multi-Purpose Disinfecting Solution is a contact lens care product, not an in vitro diagnostic device.
N/A
Intended Use / Indications for Use
For use in the daily cleaning, removing protein deposits, rinsing, chemical (not heat) disinfection and storage of soft (hydrophilic) contact lenses (including silicone hydrogel lenses) as recommended by your eye care practitioner.
OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution can also be used as a diluent for OPTI-FREE® SUPRACLENS® Daily Protein Remover.
Product codes
86 LPN
Device Description
OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution is a sterile, buffered, isotonic, aqueous solution containing sodium citrate, sodium chloride, boric acid, sorbitol, AMP-95, TETRONIC® 1304, with edetate disodium 0.05%, POLYQUAD® (polyquaternium-1) 0.001% and ALDOX™ (myristamidopropyl dimethylamine) 0.0005% as preservatives.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
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
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Cleaning Studies: A study demonstrated the ability of the product to clean lenses during soaking. The study was done to demonstrate the contribution of the rinse vs. soaking steps to the levels of lysozyme. Elimination of the post-disinfection rinse showed minimal effect on the total amount of lysozyme removed on group IV lenses. This study demonstrates the superiority of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution over Bausch & Lomb's ReNu Multi-Plus® Multi-Purpose Solution in removing protein from lenses.
Microbiology Studies: A study was conducted to evaluate the performance of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution in a regimen consisting of a 5 second rinse of lenses per side and soaking the lenses for 6 hours. No rubbing step or final rinse step was used. The results show that OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution evaluated by the test regimen (i.e., lenses rinsed for 5 seconds per lens surface and soaking for 6 hours) meets the FDA guidelines and the ISO 14729:2001 Regimen Test Requirements.
Stand Alone Test: The antimicrobial activity of OPTI-FREE Express FID 90746 was previously evaluated by the ISO 14729 (FDA 510[k]) Stand Alone Test procedure for disinfection of contact lenses (K001214). The results showed that OPTI-FREE Express FID 90746 (no soil) met the primary criteria of the Stand Alone Test. The results also showed that organic soil has no deleterious effect on the antimicrobial activity of OPTI-FREE Express FID 90746 (K001214).
Regimen Test: Previously, No Rub™ OPTI-FREE Express® was tested and passed the ISO 14729 (FDA 510 [k]) Regimen Test using the approved labeling (i.e., five second rinse per lens surface, six hour soak, and five second rinse per lens surface [no rubbing step]) (K001214). In a new study, OPTI-FREE Express FID 90746 was tested by the Regimen Test using a similar regimen, but with less rinsing of the lens ( five second rinse per lens surface and six hour soak [no rubbing and no final rinse steps]). The OPTI-FREE Express FID 90746 Investigational Regimen met the criteria of the ISO 14729 (FDA 510[k]) Regimen Test. It was concluded that the OPTI-FREE Express FID 90746 Investigational Regimen provides effective disinfection of contact lenses based on ISO 14729 and the FDA 510(k) performance criteria for contact lens disinfectants.
Clinical Study: A 30-day, randomized concurrently controlled, observer-masked (investigator and chemical analyst) and patient-masked, parallel group, multi-site study was conducted to demonstrate the safety and efficacy of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution. OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution was used with the modified directions for use. The control used in the study was Bausch & Lomb ReNu Multi-Plus® Multi-Purpose Solution. This study demonstrated the safety and efficacy of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution with a rinse/soak regimen. Significantly less residual lysozyme was found on Group IV lenses from subjects in the OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution regimen compared to lenses from subjects in the ReNu Multi-Plus® Multi-Purpose Solution group on Day 30.
Biocompatibility Testing: OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution meets the guidelines set forth in FDA's May 1, 1997 Guidance for Industry; Premarket Notification 510(k) Guidance Document for Contact Lens Care Products. OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution remains unchanged from the previously approved product (P830034/S32, K973332) except for the labeling change revising the directions for use. The labeling changes require no new biocompatibility testing.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
K973332, K974624, K983780, K001214, K002589
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 886.5928 Soft (hydrophilic) contact lens care products.
(a)
Identification. A soft (hydrophilic) contact lens care product is a device intended for use in the cleaning, rinsing, disinfecting, lubricating/rewetting, or storing of a soft (hydrophilic) contact lens. This includes all solutions and tablets used together with soft (hydrophilic) contact lenses and heat disinfecting units intended to disinfect a soft (hydrophilic) contact lens by means of heat.(b)
Classification. Class II (Special Controls) Guidance Document: “Guidance for Industry Premarket Notification (510(k)) Guidance Document for Contact Lens Care Products.”
0
510(K) SUMMARY
Submitted by:
Ralph H. Larsen Sr. Manager, Regulatory Affairs Alcon Research, Ltd. 6201 South Freeway Fort Worth, Texas 76134-2099 (817) 551-4702 (Phone) (817) 551-4630 (Fax)
Device Name:
| Common Name: | Contact Lens Care Multi-Purpose Disinfecting Solution |
|---|---|
| Proprietary Name: | OPTI-FREE® EXPRESS® Multi-Purpose Disinfecting Solution |
Indications for Use:
For use in the daily cleaning, removing protein deposits, rinsing, chemical (not heat) disinfection and storage of soft (hydrophilic) contact lenses (including silicone hydrogel lenses) as recommended by your eye care practitioner.
OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution can also be used as a diluent for OPTI-FREE® SUPRACLENS® Daily Protein Remover.
1
Description:
OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution is a sterile, buffered, isotonic, aqueous solution containing sodium citrate, sodium chloride, boric acid, sorbitol, AMP-95, TETRONIC® 1304, with edetate disodium 0.05%, POLYQUAD® (polyquaternium-1) 0.001% and ALDOX™ (myristamidopropyl dimethylamine) 0.0005% as preservatives.
Substantial Equivalence:
OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution is substantially equivalent, in terms of its actions and indications for use, to OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution, cleared for marketing under 510(k) K973332 (originally submitted as P830034/S32), K974624, K983780, K001214 (no rub directions for use for lenses replaced within 30 days or less) and K002589 (no rub directions for all lenses). OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution meets the guidelines set forth in FDA's May 1, 1997 Guidance for Industry; Premarket Notification 510(k) Guidance Document for Contact Lens Care Products.
Safety and Effectiveness:
Cleaning Studies
A study demonstrated the ability of the product to clean lenses during soaking. The study was done to demonstrate the contribution of the rinse vs. soaking steps to the levels of lysozyme. Elimination of the post-disinfection rinse showed minimal effect on the total amount of lysozyme removed on group IV lenses. This study demonstrates the superiority of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution over Bausch & Lomb's ReNu Multi-Plus® Multi-Purpose Solution in removing protein from lenses.
2
Microbiology Studies
A study was conducted to evaluate the performance of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution in a regimen consisting of a 5 second rinse of lenses per side and soaking the lenses for 6 hours. No rubbing step or final rinse step was used. The results show that OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution evaluated by the test regimen (i.e., lenses rinsed for 5 seconds per lens surface and soaking for 6 hours) meets the FDA guidelines and the ISO 14729:2001 Regimen Test Requirements.
Stand Alone Test:
The antimicrobial activity of OPTI-FREE Express FID 90746 was previously evaluated by the ISO 14729 (FDA 510[k]) Stand Alone Test procedure for disinfection of contact lenses (K001214). The results showed that OPTI-FREE Express FID 90746 (no soil) met the primary criteria of the Stand Alone Test. The results also showed that organic soil has no deleterious effect on the antimicrobial activity of OPTI-FREE Express FID 90746 (K001214).
Regimen Test:
Previously, No Rub™ OPTI-FREE Express® was tested and passed the ISO 14729 (FDA 510 [k]) Regimen Test using the approved labeling (i.e., five second rinse per lens surface, six hour soak, and five second rinse per lens surface [no rubbing step]) (K001214). In a new study, OPTI-FREE Express FID 90746 was tested by the Regimen Test using a similar regimen, but with less rinsing of the lens ( five second rinse per lens surface and six hour soak [no rubbing and no final rinse steps]).
3
The OPTI-FREE Express FID 90746 Investigational Regimen met the criteria of the ISO 14729 (FDA 510[k]) Regimen Test.
It was concluded that the OPTI-FREE Express FID 90746 Investigational Regimen provides effective disinfection of contact lenses based on ISO 14729 and the FDA 510(k) performance criteria for contact lens disinfectants.
Clinical Study
A 30-day, randomized concurrently controlled, observer-masked (investigator and chemical analyst) and patient-masked, parallel group, multi-site study was conducted to demonstrate the safety and efficacy of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution. OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution was used with the modified directions for use. The control used in the study was Bausch & Lomb ReNu Multi-Plus® Multi-Purpose Solution.
This study demonstrated the safety and efficacy of OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution with a rinse/soak regimen.
Significantly less residual lysozyme was found on Group IV lenses from subjects in the OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution regimen compared to lenses from subjects in the ReNu Multi-Plus® Multi-Purpose Solution group on Day 30.
Biocompatibility Testing
OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution meets the guidelines set forth in FDA's May 1, 1997 Guidance for Industry; Premarket Notification 510(k) Guidance Document for Contact Lens Care Products.
4
OPTI-FREE EXPRESS Multi-Purpose Disinfecting Solution remains unchanged from the previously approved product (P830034/S32, K973332) except for the labeling change revising the directions for use. The labeling changes require no new biocompatibility testing.
.
5
Image /page/5/Picture/1 description: The image shows the logo for the Department of Health & Human Services USA. The logo features a stylized image of an eagle with three faces in profile, all facing to the right. The eagle is positioned to the right of the text, which is arranged in a circular pattern around the logo. The text reads "DEPARTMENT OF HEALTH & HUMAN SERVICES USA".
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
AUG 0 8 2002
Alcon Research, LTD c/o Ralph H. Larsen Sr. Manager, Regulatory Affairs 6201 South Freeway Fort Worth, TX 76134-2099
Re: K021143
Trade/Device Name: OPTI-FREE EXPRESS® Multipurpose Disinfecting Solution (Modifed Directions for Use) Regulation Number: 21 CFR 886.5928 Regulation Name: Soft (hydrophilic) Contact Lens Care Products Regulatory Class: Class II Product Code: 86 LPN Dated: June 18, 2002 Received: June 20, 2002
Dear Mr. Larsen:
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.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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.
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); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
6
Page 2 -- Mr. Ralph Larsen
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4613. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
A. Ralph Rosenthal
A. Ralph Rosenthal, M.D. Director Division of Ophthalmic and Ear, Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health
7
510(k) Number (if known): K021143
Device Name: OPTI-FREE® EXPRESS® Multi-Purpose Disinfecting Solution
Indications for Use:
For use in the daily cleaning, removing protein deposits, rinsing, chemical (not heat) disinfection and storage of soft (hydrophilic) contact lenses (including silicone hydrogel lenses) as recommended by your eye care practitioner.
OPTI-FREE® EXPRESS® Multi-Purpose Disinfecting Solution can also be used as a diluent for OPTI-FREE® SUPRACLENS® Daily Protein Remover.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Myra Smith
510(k) Number K021143
Prescription Use
(Per 21 CFR 801.109)
OR
Over-The Counter Use