Philips received FDA 510(k) clearance for a sensor.

2 reports, 2 independent Updated Sep 3

Gone quiet

Reports: 2
Developments: 2
Repetition: 0%

New informationRepeats or wire copies

AI-generated analysis. Brind wrote this summary from the reports listed below. It can be wrong. Each section says how much you can rely on it, and the sources are linked so you can check.

What happened

Some supportReported by 2 outlets

Philips received FDA 510(k) clearance for a sensor.

Who's involved

What this event is mainly about

FDA Koninklijke Philips NV

How it developed

Newest first. Tap a step to see who reported it.

Sep 3Philips' eV14-2v transducer received FDA 510(k) clearance and CE marks.1 source
- finanznachrichten.de
Jul 21Philips secured FDA 510(k) clearance for a new sensor device.1 source
- manilatimes.net

Keep exploring

Part of

Philips products received FDA-cleared AI enhancements, with the company being a global leader based in the Netherlands. All 2 developments

The entities involved

FDA
- Generic medicine services are seeking approval for launch from the FDA.Mon 17:49
- A company is seeking FDA feedback on its NEO212 program, with a meeting scheduled at the FDA's White Oak campus.Mon 14:56
Koninklijke Philips NV
Dutch multinational conglomerate corporation

Nothing else this week.

Coverage

Newest first; wire copies grouped

Sep 3finanznachrichten.de
Jul 21manilatimes.net