Medical Device Manufacturer · US , Petaluma , CA

Spectrum Antimicrobials, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

Spectrum Antimicrobials, Inc. has 1 FDA 510(k) cleared medical devices. Based in Petaluma, US.

Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Spectrum Antimicrobials, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Dunn Regulatory Associates, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Spectrum Antimicrobials, Inc.
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