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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K220301

Volumat Line · Fresenius Kabi · decided 2023-06-02 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Volumat™ LineVL PR 42-12Fresenius Kabi AGFRN04250273714357
Volumat™ LineVL ON72-X1Fresenius Kabi AGFRN04250273731866
Volumat™ LineVL ON 72-1Fresenius Kabi AGFRN04250273714395
Volumat™ LineVL SP 62-1Fresenius Kabi AGFRN04250273714838
Volumat™ LineVL PR 42-21Fresenius Kabi AGFRN04250273714296
Volumat™ LineVL SP40-11Fresenius Kabi AGFRN04250273733860
Volumat™ LineVL ST02-X0Fresenius Kabi AGFRN04250273731842
Volumat™ LineVL PR 72-11Fresenius Kabi AGFRN04250273714333
Volumat™ Line VL ST 02-0Fresenius Kabi AGFRN04250273714272
Volumat™ LineVL PA 92-2Fresenius Kabi AGFRN04250273714319
Volumat™ LineVL SP 22-0 Fresenius Kabi AGFRN04250273714180
Volumat™ LineVL PR 42-11Fresenius Kabi AGFRN04250273714258
Volumat™ LineVL PA 92-1Fresenius Kabi AGFRN04250273714494
Volumat™ LineVL PN 02-1Fresenius Kabi AGFRN04250273714371
Volumat™ LineVL PR44-12Fresenius Kabi AGFRN04250273731965