Biomoneta Avata Rx

FDA 510(k) K251872 · Biomoneta Research Private Limited

Substantially Equivalent

510(k) numberK251872

Submission

Device name
Biomoneta Avata Rx
Applicant
Biomoneta Research Private Limited
Bengaluru, IN
Received
June 18, 2025
Decision date
November 14, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FRF – Cleaner, Air, Medical Recirculating
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5045
Specialty
General Hospital

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Questions and answers

When was Biomoneta Avata Rx cleared by the FDA?

Biomoneta Avata Rx (K251872) received a 510(k) decision of Substantially Equivalent on November 14, 2025, 149 days after the submission was received.

What is the product code of K251872?

The FDA product code is FRF – Cleaner, Air, Medical Recirculating, a Class II (moderate risk) device regulated under 21 CFR 880.5045.