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Device, Biopsy, Endomyocardial
FDA product code DWZ · Class 2 · Cardiovascular
77
Registered devices
89
Adverse events
1
Recalls
23
510(k) clearances
Devices with this code
SparrowHawk — ATC TECHNOLOGIES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.NA — Fehling Instruments GmbH & Co. KGBIOPSY FORCEPS STD — Cordis US Corp.NA — Fehling Instruments GmbH & Co. KGNovatome™ — Merit Medical Systems, Inc.ultraCbx — Lake Region MedicalNA — Fehling Instruments GmbH & Co. KGNovatome — SCHOLTEN SURGICAL INSTRUMENTS, INC.Procure™ — ST. JUDE MEDICAL, INC.Jawz Endomyocardial Biopsy Forceps — ARGON MEDICAL DEVICES, INC.NA — Fehling Instruments GmbH & Co. KGJawz Endomyocardial Biopsy Forceps — ARGON MEDICAL DEVICES, INC.Novatome™ — Merit Medical Systems, Inc.SparrowHawk — ATC TECHNOLOGIES, INC.Jawz Endomyocardial Biopsy Forceps — ARGON MEDICAL DEVICES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.Jawz Endomyocardial Biopsy Forceps — ARGON MEDICAL DEVICES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.Procure™ — ST. JUDE MEDICAL, INC.Novatome — SCHOLTEN SURGICAL INSTRUMENTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-12 | Heartport, Inc. | Guidewire is protruding through the film portion of the packages which compromises the sterility of the device. |
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