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510(k) Data Aggregation
(54 days)
The J-Tip Needleless Injector system is used for the subcutaneous administration of medications which are appropriate to deliver by jet injection.
J-Tip Needles Injector
Apologies, but the provided text from the FDA 510(k) letter for the "J-Tip Needleless Injector" does not contain the information requested regarding acceptance criteria and details of a study proving device performance.
The document is a substantial equivalence determination letter, which means the FDA has determined that the J-Tip Needleless Injector is as safe and effective as a legally marketed predicate device. This letter typically does not include the detailed study methodology, acceptance criteria, or performance data that would be found in a 510(k) summary or the actual submission itself.
Therefore, I cannot provide the specific details you've asked for based on the input document, such as:
- A table of acceptance criteria and reported device performance.
- Sample sizes or data provenance.
- Number or qualifications of experts for ground truth.
- Adjudication method.
- MRMC comparative effectiveness study results.
- Standalone performance details.
- Type of ground truth used.
- Training set details.
- Ground truth establishment for the training set.
The letter focuses on the regulatory decision and the device's classification, not the technical study details.
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