Light Diagnostics Human Metapneumovirus Dfa Kit, Model Catalog Number 3124

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K093815 ↗

FDA Product Code

OMG

FDA applicant

Millipore Corporation

Device Class

Class II

Regulation

21 CFR Part 866.3980

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

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• Ultra-Free

  Class I

  FDA 510(k) K790445 Active Cleared 28 Jun 1979

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See all devices from Millipore Corp. →