(28 days)
No
The document describes contact lenses for vision correction and eye color enhancement. There is no mention of any software, algorithms, or data processing that would indicate the use of AI or ML. The description focuses on the physical properties, materials, and intended use of the lenses.
No.
The device is used for optical correction of refractive ametropia (myopia, hyperopia, astigmatism, presbyopia) and for cosmetic purposes to enhance or alter eye color, which are not considered therapeutic treatments.
No
Explanation: The document states that the device is intended for "optical correction of refractive ametropia" and "enhancement or alteration of the apparent color of the eye," which are therapeutic/cosmetic functions, not diagnostic ones. There is no mention of the device being used to identify or detect medical conditions.
No
The device description clearly indicates that the device is a physical contact lens made of nelfilcon A material, with specific physical properties and designs. It is not a software-only device.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for the optical correction of refractive errors (myopia, hyperopia, astigmatism, presbyopia) and to enhance or alter the apparent color of the eye. This is a therapeutic and cosmetic purpose, not a diagnostic one.
- Device Description: The description focuses on the material composition, physical properties, and design of the contact lenses. It does not mention any components or functions related to analyzing samples from the human body for diagnostic purposes.
- Performance Studies: The performance studies mentioned are related to biocompatibility, process validation, and equivalence to predicate devices, which are typical for medical devices, but not specifically for IVDs. There are no mentions of studies evaluating the device's ability to detect or measure substances or conditions in a biological sample.
IVD devices are specifically designed to examine specimens derived from the human body (like blood, urine, tissue) to provide information for the diagnosis, prevention, monitoring, treatment, or alleviation of disease. The DAILIES Colors contact lenses do not perform this function.
N/A
Intended Use / Indications for Use
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses with refractive power, are indicated for the optical correction of refractive ametropia (myopia, hyperopia ) in not-aphakic persons with up to approximately 1.50 diopters (D) of astigmatism that does not interfere with visual acuity.
DAILIES® Colors Toric (nelfilcon A) One-Day Contact Lenses are indicated for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in not-aphakic persons with non-diseased eyes with 6.00 diopters (D) or less of astigmatism.
DAILIES® Colors Progressives (nelfilcon A) One-Day Contact Lenses are indicated for the optical correction of presbyopia, with or without refractive ametropia (myopia and hyperopia) in not-aphakic persons with non-diseased eyes who may require a reading addition of +3.00 diopters (D) or less and who may have 2.00 diopters (D) or less of astigmatism that does not interfere with visual acuity.
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses (with or without corrective power) also act to enhance or alter the apparent color of the eye.
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses are to be prescribed for single-use daily disposable wear (less than 24 hours while awake) only. The lenses are not intended to be cleaned or disinfected and should be discarded after a single use.
Product codes
LPL, MVN
Device Description
The subject device, DAILIES Colors contact lenses, are a modification of the currently commercialized FreshLook® One-Day (nelfilcon A) color contact lenses. DAILIES Colors are soft contact lenses intended for the optical correction of refractive error, and the enhancement or alteration of the apparent color of the eye. Geometries include spherical, toric, and multifocal lens designs.
DAILIES Colors lenses are composed of nelfilcon A, which is a non-ionic, hydrophilic lens material, that consists of approximately 69% water and 31% PVA (polyviny) alcohol partially acetalized with N-formylmethyl acrylamide). The lenses are pad printed with intermittent ink layers containing a combination of the following color additives, approved for use in color contact lenses: chromium oxide, iron oxides, [phthalocyaninato (2- )] copper, phthalocyanine green, and titanium dioxide.
Lens designs for DAILIES Colors (nelfilcon A) lenses include spherical, toric, and multifocal lenses in the following parameter range:
• Diameter Range: 13.0 to 15.0 mm
• Base Curve Range: 8.0 to 9.2 mm
• Power Range: -20.00D to +20.00D
• Center Thickness: varies with design and power (0.100 mm for -3.00D spherical)
Lenses have the following properties:
• Refractive index: 1.38 (hydrated)
• Water content: 69% by weight in normal saline
• Oxygen permeability 26 barrer units at 35 °C (Fatt corrected)
• % Light transmittance > 88% (average over 380-780 nm)
Lenses are provided in sterile packages of foil-sealed blister-packs containing buffered saline.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
eyes
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Prescription Use
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)
Performance testing was conducted in consideration of the May 1994 FDA Guidelines entitled Premarket Notification 510(k) Guidance Document for Class II Contact Lenses. The modified device underwent a successful process validation to verify equivalence to the predicate device. Results met the acceptance criteria accordingly.
Non-clinical testing: Successful biocompatibility testing as well as process validation were completed for the modified device to verify equivalence to the predicate device. This resulted in all acceptance criteria being met. Stability testing for the predicate device continues to support the labeled expiration date.
Clinical testing: The scope of the device modification did not necessitate clinical testing, in order to establish safety or efficacy.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 886.5925 Soft (hydrophilic) contact lens.
(a)
Identification. A soft (hydrophilic) contact lens is a device intended to be worn directly against the cornea and adjacent limbal and scleral areas of the eye to correct vision conditions or act as a therapeutic bandage. The device is made of various polymer materials the main polymer molecules of which absorb or attract a certain volume (percentage) of water.(b)
Classification. (1) Class II if the device is intended for daily wear only.(2) Class III if the device is intended for extended wear.
(c)
Date PMA or notice of completion of a PDP is required. As of May 28, 1976, an approval under section 515 of the act is required before a device described in paragraph (b)(2) of this section may be commercially distributed. See § 886.3.
0
Image /page/0/Picture/0 description: The image contains the logos of the Department of Health & Human Services and the Food and Drug Administration (FDA). The Department of Health & Human Services logo is on the left, and the FDA logo is on the right. The FDA logo includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text.
February 6, 2019
Alcon Laboratories, Inc. Heather Smith Regulatory Affairs Specialist 6201 South Freeway Fort Worth, TX 76134-2099
Re: K190045
Trade/Device Name: DAILIES® Colors, DAILIES® Colors Toric, DAILIES® Colors Progressives Alternate family trade name: FreshLook® One-Day color contact lenses Regulation Number: 21 CFR 886.5925 Regulation Name: Soft (Hydrophilic) Contact Lens Regulatory Class: Class II Product Code: LPL, MVN Dated: January 3, 2019 Received: January 9, 2019
Dear Heather Smith:
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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.
1
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) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see
https://www.fda.gov/CombinationProducts/GuidanceRegulatoryInformation/ucm597488.htm); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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 comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely.
J Angelo Green -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
2
Indications for Use
510(k) Number (if known) K190045
Device Name
DAILIES® Colors; DAILIES® Colors Toric; DAILIES® Colors Progressives Alternate family trade name: FreshLook® One-Day color contact lenses
Indications for Use (Describe)
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses with refractive power, are indicated for the optical correction of refractive ametropia (myopia, hyperopia ) in not-aphakic persons with up to approximately 1.50 diopters (D) of astigmatism that does not interfere with visual acuity.
DAILIES® Colors Toric (nelfilcon A) One-Day Contact Lenses are indicated for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in not-aphakic persons with non-diseased eyes with 6.00 diopters (D) or less of astigmatism.
DAILIES® Colors Progressives (nelfilcon A) One-Day Contact Lenses are indicated for the optical correction of presbyopia, with or without refractive ametropia (myopia and hyperopia) in not-aphakic persons with non-diseased eyes who may require a reading addition of +3.00 diopters (D) or less and who may have 2.00 diopters (D) or less of astigmatism that does not interfere with visual acuity.
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses (with or without corrective power) also act to enhance or alter the apparent color of the eye.
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses are to be prescribed for single-use daily disposable wear (less than 24 hours while awake) only. The lenses are not intended to be cleaned or disinfected and should be discarded after a single use.
Type of Use (Select one or both, as applicable)
| Prescription Use (Part 21 CFR 801 Subpart D) | |
|---|---|
| Over-The-Counter Use (21 CFR 801 Subpart C) |
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510(k) Summary
This 510(k) summary document has been prepared in accordance with section 21 CFR 807.92.
I. Submitter of the 510(k)
| Company: | Alcon Laboratories, Inc.
6201 South Freeway
Fort Worth, TX 76134-2099, USA |
|-------------------------|----------------------------------------------------------------------------------|
| Primary Contact Person: | Heather Smith |
| Phone: | (678) 415-6884 |
| Fax: | n/a |
| Email: | Heather.Smith@alcon.com |
| Back up Contact Person: | Martina Heim |
| Phone: | (678) 415 3565 |
| Fax: | n/a |
| Email: | Martina.Heim@alcon.com |
| Date Prepared: | 03 January 2019 |
II. Devices Subject to this 510(k)
| Trade Names: | DAILIES® Colors |
|---|---|
| DAILIES® Colors Progressives | |
| DAILIES® Colors Toric | |
| Alternate family trade name: FreshLook® One-Day color | |
| contact lenses | |
| Common Name: | Soft Contact Lens |
| Classification Name: | Soft (Hydrophilic) Contact Lens [for daily wear] |
| Device Classification: | Class II [21 CFR 886.5925 (b)(1)] |
| Product Code: | LPL, MVN |
4
III. Predicate Device
The predicate lens FreshLook® One-Day (nelfilcon A) colors contact lenses received FDA clearance under Premarket Notification 510(k) K050213, with recent updates cleared under K180398 and K180669.
Device Description IV.
The subject device, DAILIES Colors contact lenses, are a modification of the currently commercialized FreshLook® One-Day (nelfilcon A) color contact lenses. DAILIES Colors are soft contact lenses intended for the optical correction of refractive error, and the enhancement or alteration of the apparent color of the eye. Geometries include spherical, toric, and multifocal lens designs.
DAILIES Colors lenses are composed of nelfilcon A, which is a non-ionic, hydrophilic lens material, that consists of approximately 69% water and 31% PVA (polyviny) alcohol partially acetalized with N-formylmethyl acrylamide). The lenses are pad printed with intermittent ink layers containing a combination of the following color additives, approved for use in color contact lenses: chromium oxide, iron oxides, [phthalocyaninato (2- )] copper, phthalocyanine green, and titanium dioxide.
Lens designs for DAILIES Colors (nelfilcon A) lenses include spherical, toric, and multifocal lenses in the following parameter range:
| • Diameter Range: | 13.0 to 15.0 mm |
|---|---|
| • Base Curve Range: | 8.0 to 9.2 mm |
| • Power Range: | -20.00D to +20.00D |
| • Center Thickness: | varies with design and power |
| (0.100 mm for -3.00D spherical) |
Lenses have the following properties:
| • Refractive index: | 1.38 (hydrated) |
|---|---|
| • Water content: | 69% by weight in normal saline |
| • Oxygen permeability | 26 barrer units at 35 °C (Fatt corrected) |
| • % Light transmittance | > 88% (average over 380-780 nm) |
5
Lenses are provided in sterile packages of foil-sealed blister-packs containing buffered saline.
V. Indications for Use
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses, with refractive power, are indicated for the optical correction of refractive ametropia (myopia and hyperopia ) in not-aphakic persons with non-diseased eyes with up to approximately 1.50 diopters (D) of astigmatism that does not interfere with visual acuity.
DAILIES® Colors Toric (nelfilcon A) One-Day Contact Lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in not-aphakic persons with nondiseased eyes with 6.00 diopters (D) or less of astigmatism.
DAILIES® Colors Progressives (nelfilcon A) One-Day Contact Lenses are indicated for the optical correction of presbyopia, with or without refractive ametropia (myopia and hyperopia), in not-aphakic persons with non-diseased eyes who may require a reading addition of +3.00 diopters (D) or less and who may have 2.00 diopters (D) or less of astigmatism that does not interfere with visual acuity.
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses (with or without corrective power) also act to enhance or alter the apparent color of the eye.
DAILIES® Colors (nelfilcon A) One-Day Contact Lenses are to be prescribed for single-use daily disposable wear (less than 24 hours while awake) only. The lenses are not intended to be cleaned or disinfected and should be discarded after a single use.
VI. Comparison to Technological Characteristics with the Predicate Device
The design modification for DAILIES Colors involves addition of a modified print pattern, with a larger, more pronounced outer diameter and a less pronounced inner print pattern, utilizing the same, currently approved color additives as applied in FreshLook One-Day color contact lenses.
The following table summarizes the characteristics of the modified device as compared to the commercially available predicate device.
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| Predicate Device | Modified Device | |
|---|---|---|
| Trade Name (brand) | FreshLook® One-Day | Additional (alternate) trade name: |
| DAILIES® Colors | ||
| 510(k) | K050213 | K190045 |
| Device Classification | ||
| Information | Class II [21 CFR 886.5925 (b)(1)] | Same |
| Intended Use | With refractive power: | |
| Vision correction | ||
| With or without refractive power: | ||
| Enhancement or alteration of the | ||
| apparent color of the eye | Same | |
| Wearing schedule | Daily wear | Same |
| Replacement schedule | Daily disposable | Same |
| Material Classification | Group 2 | |
| (>50% H2O, nonionic polymer), | ||
| according to ISO 18369-1: 2017 | Same | |
| Lens Material | Nelfilcon A | Same |
| Power Range | -20.00D to +20.00D | Same |
| Print technology | In-mold pad print technology | Same |
| Color Additives | Chromium Oxide, Iron oxides, | |
| [phthalocyaninato (2- )] copper, | ||
| phthalocyanine green, Titanium | ||
| Dioxide | Same | |
| Water Content | 69%, by weight | Same |
| Light Transmittance | > 88%T | Same |
| Refractive Index | 1.38 | Same |
| Oxygen Permeability | 26 barrer units @ 35 °C | Same |
| Manufacturing Method | Lightstream Technology: | |
| Full mold cast, integrated print step | Same | |
| Sterilization | Steam sterilization in validated | |
| autoclave | Same | |
| Biocompatibility | Biocompatible as confirmed by | |
| appropriate biocompatibility testing | Same | |
| Packaging | Blister pack | Same |
| Package Storage Saline | ||
| Solution | Phosphate-acetate buffered saline | |
| solution with up to 0.05% | ||
| Poloxamer 108 | Same |
Table 1: Substantial Equivalence Comparison
7
In accordance with the criteria for claims of substantial equivalence in the FDA Guidance document Premarket Notification 510(k) Guidance Document for Daily Wear Contact Lenses, May 1994, the information provided herein supports the claim of substantial equivalence to the lens with an existing USAN name and the same manufacturing process.
VII. Performance Data
Performance testing was conducted in consideration of the May 1994 FDA Guidelines entitled Premarket Notification 510(k) Guidance Document for Class II Contact Lenses. The modified device underwent a successful process validation to verify equivalence to the predicate device. Results met the acceptance criteria accordingly.
Non-clinical testing
Successful biocompatibility testing as well as process validation were completed for the modified device to verify equivalence to the predicate device. This resulted in all acceptance criteria being met.
Stability testing for the predicate device continues to support the labeled expiration date.
Clinical testing
The scope of the device modification did not necessitate clinical testing, in order to establish safety or efficacy.
Substantial Equivalence
DAILIES® Colors, DAILIES® Colors Toric, and DAILIES® Colors Progressives (nelfilcon A) one-day contact lenses are substantially equivalent to the predicate lenses and similar to other daily wear contact lenses, in terms of water content (69% water, by weight) and ionic characteristics (FDA Group II (>50% H2O, non-ionic polymer)).
VIII. Conclusions
The cumulative results of all performance testing demonstrate the safety, efficacy, and performance of the modified device and thus, the substantial equivalence to the predicate device.
DAILIES Colors (nelfilcon A) one day contact lenses, with a modified print pattern, are substantially equivalent to the predicate lens in terms of material properties, biocompatibility, clinical performance, and indications for use.