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510(k) Data Aggregation
K Number
K972157Device Name
EXCEL AV STIM 1000Manufacturer
Date Cleared
1998-01-30
(235 days)
Product Code
Regulation Number
882.1900Type
TraditionalPanel
NeurologyReference & Predicate Devices
N/A
Why did this record match?
Device Name :
EXCEL AV STIM 1000
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
AUDITORY TO PROVIDE VISUAL AND RECORDING FOR STIMULI EVOKED POTENTIAL S
Device Description
Not Found
AI/ML Overview
I am sorry, but the provided text does not contain the acceptance criteria or a study proving that a device meets the acceptance criteria. The document is a clearance letter from the FDA for a device called "Excel AV Stim 1000" (later referred to as "Excel AV Stim 4000" in the Indications For Use section), stating that it is substantially equivalent to legally marketed predicate devices.
The document includes:
- Trade Name: Excel AV Stim 1000 (and 4000)
- Regulatory Class: II
- Product Code: GWJ
- Indications For Use: "AUDITORY TO PROVIDE VISUAL AND RECORDING FOR STIMULI EVOKED POTENTIAL S"
However, it does not provide any information about:
- A table of acceptance criteria and reported device performance.
- Sample size used for a test set or data provenance.
- Number of experts used to establish ground truth or their qualifications.
- Adjudication method for a test set.
- A multi-reader multi-case (MRMC) comparative effectiveness study or its effect size.
- Standalone performance of an algorithm.
- The type of ground truth used.
- Sample size for a training set.
- How the ground truth for the training set was established.
Therefore, I cannot fulfill your request based on the provided text.
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