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Carex Hybrid Personal Lubricant is a personal lubricant. for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity and supplement the body's natural lubrication. This product is compatible with natural rubber latex, and polyisoprene condoms. This product is not compatible with polyurethane condoms

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This document is not about an AI/ML device but rather a 510(k) clearance for a personal lubricant. It does not contain information on acceptance criteria for an AI device, performance studies, sample sizes, expert ground truth, or MRMC studies. Therefore, I cannot fulfill your request based on the provided text.

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Karex's water based personal lubricant with flavors is a personal lubricant, for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity and supplement the body's natural lubrication. This product is compatible with natural rubber latex condoms. This product is not compatible with polyisoprene and polyurethane condoms.

Water Based Personal Lubricant with Flavors

• Vanilla
• Aloe Vera
• Strawberry
• Banana
• Peppermint
• Chocolate

This document is a 510(k) premarket notification decision letter from the FDA to Karex Industries Sdn. Bhd. for a "Water Based Personal Lubricant with Flavors." The letter states that the device is substantially equivalent to legally marketed predicate devices.

Crucially, this document pertains to a medical device approval for a lubricant, not a study evaluating an AI-powered diagnostic device. As such, the information requested for acceptance criteria and study details (e.g., test set, training set, expert consensus, MRMC studies) is not present in this document. The document primarily discusses regulatory compliance and the FDA's substantial equivalence determination for a physical product.

Therefore, I cannot provide the requested information based on the provided text. The document does not contain data or information about:

1. A table of acceptance criteria and reported device performance for an AI/diagnostic device.
2. Sample sizes, data provenance, ground truth establishment for test or training sets.
3. Number and qualifications of experts.
4. Adjudication methods.
5. MRMC studies or effect sizes for human readers.
6. Standalone algorithm performance.
7. Type of ground truth used (e.g., pathology, outcomes data).

The text is about the regulatory approval of a personal lubricant.

Ask a specific question about this device