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Bio-Med Devices, Inc.

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Bio Med Devices Patient Breathing Circuit Catalog Number: 80011 Labeled in part: '':PATIEN recall (Z-0423-05)Bio-Med Devices, Inc.2005-01-29
Bio Med Devices Patient Breathing Circuit Catalog Number: 80015 Labeled in part: DO NOT RE recall (Z-0424-05)Bio-Med Devices, Inc.2005-01-29
Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part: ONE SET - recall (Z-0425-05)Bio-Med Devices, Inc.2005-01-29
Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A-7 Labeled in part: ONE SET recall (Z-0426-05)Bio-Med Devices, Inc.2005-01-29
Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A-9 Labeled in part: ONE SET recall (Z-0427-05)Bio-Med Devices, Inc.2005-01-29
Pneumotach, Disposable (B) Catalog Number: 4408 Labeled in part: SINGLE USE CATALOG NO.440 recall (Z-0428-05)Bio-Med Devices, Inc.2005-01-29
Bio-Med Patient Breathing Circuit Product NUmber: 3030-5 Labeled in part: ONE SET - SINGLE recall (Z-0429-05)Bio-Med Devices, Inc.2005-01-29
Bio-Med Dental Breathing Circuit Product NUmber: DENTL recall (Z-0430-05)Bio-Med Devices, Inc.2005-01-29
MVP-10 Pediatric/ Neonatal Volume Ventilator recall (Z-0300-04)Bio-Med Devices, Inc.2004-01-06

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Every clearance here is in the API, with alerts when new ones post.