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The Tru-Cable™ endoscopic fiber optic cable is designed to transmit light for illumination purposes from a remote source to an endoscope or similar surgical instrument. It can be adapted to be compatible with a variety of illuminators.

The Truphatek Tru-Cable™ endoscopic fiber optic cables are:

• . Lengths of 10 feet (3.5m)
• Diameters 3.5mm and 5.0mm .
• The fiber optic cable is hermetically sealed in a closed system so that it can be . sterilized or high level disinfected using most common methods.
• The cables are sold non-sterile. .
  The fiber optic cables are designed for use with all the most popular light source illuminators and surgical instruments that are equipped with standard endoscopic adapters. They are designed for user high level disinfection and / or sterilization by autoclave or high level disinfection may be done via Steris® or Liquid Chemicals, i.e. Cidex OPA®. The cable is rated for 100 uses when processed via autoclave.

This document is a 510(k) Pre-Market Notification for the Tru-Cable™ endoscopic fiber optic cables. It focuses on demonstrating substantial equivalence to predicate devices and does NOT contain information about acceptance criteria, device performance studies, sample sizes, expert ground truth establishment, adjudication methods, MRMC studies, or standalone algorithm performance.

Therefore, I cannot fulfill your request for:

1. A table of acceptance criteria and the reported device performance
2. Sample size used for the test set and the data provenance
3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts
4. Adjudication method for the test set
5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, and the effect size of human readers improving with AI vs. without AI assistance
6. If a standalone (i.e., algorithm only without human-in-the-loop performance) was done
7. The type of ground truth used
8. The sample size for the training set
9. How the ground truth for the training set was established

This device is a physical medical instrument (fiber optic cable), not an AI/software device. The 510(k) summary provided is for a traditional medical device submission, which typically focuses on bench testing, biocompatibility, sterilization validation, and comparison to legally marketed predicate devices, rather than performance metrics typically associated with AI/ML diagnostic or prognostic tools.

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