FDA product code SID: Tempo Pilot Msk: Musculoskeletal
SID is the FDA product code for tempo pilot msk: musculoskeletal. It is a Not classified device, reviewed by the Clinical Chemistry panel. Devices under SID reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
TEMPO Pilot: musculoskeletal (chronic musculoskeletal pain)
Classification
| Field | Value |
|---|---|
| Device name | Tempo Pilot Msk: Musculoskeletal |
| Device class | Not classified |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Unknown |
| Premarket route | 510(k) exempt |
Recalls for SID devices
openFDA lists no recalls for product code SID.
Frequently asked questions
What is FDA product code SID?
SID is the FDA product code for tempo pilot msk: musculoskeletal. It is a Not classified device, reviewed by the Clinical Chemistry panel.
What device class is SID?
Not classified. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code SID
- Run a recall and safety report across every SID manufacturer
- Watch product code SID for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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