Home › Device types › DWZ
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
ultraCbx — Lake Region MedicalNovatome — SCHOLTEN SURGICAL INSTRUMENTS, INC.NA — Fehling Instruments GmbH & Co. KGNA — Fehling Instruments GmbH & Co. KGSparrowHawk — ATC TECHNOLOGIES, INC.Cook — COOK INCORPORATEDSparrowHawk — ATC TECHNOLOGIES, INC.Jawz Endomyocardial Biopsy Forcep — ARGON MEDICAL DEVICES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.NA — Fehling Instruments GmbH & Co. KGNA — Fehling Instruments GmbH & Co. KGSparrowHawk — ATC TECHNOLOGIES, INC.Jawz Endomyocardial Biopsy Forceps — ARGON MEDICAL DEVICES, INC.SparrowHawk — ATC TECHNOLOGIES, INC.Novatome — SCHOLTEN SURGICAL INSTRUMENTS, INC.NA — Fehling Instruments GmbH & Co. KGSparrowHawk — ATC TECHNOLOGIES, INC.Jawz Endomyocardial Biopsy Forceps — ARGON MEDICAL DEVICES, INC.NA — Fehling Instruments GmbH & Co. KGultraCbx — Lake Region MedicalNovatome™ — Merit Medical Systems, Inc.Biopsy Forceps — CORDIS CORPORATIONJawz Endomyocardial Biopsy Forceps — ARGON MEDICAL DEVICES, INC.Novatome™ — Merit Medical Systems, 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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.