Device, Biopsy, Endomyocardial
FDA product code DWZ · 23 cleared devices
Class 2
Cardiovascular
- Regulation
- 21 CFR 870.4075
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1981-04-17 – 2025-09-30
DWZ
2025-09-30
DWZ
2017-06-02
Biopsy Forceps
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DWZ
2007-10-03
NOVATOME, MODEL: SU101-50
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DWZ
2001-06-06
SPARROWHAWK DISPOSABLE
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DWZ
2000-02-28
MODIFICATION TO T-REX BIOPSY FORCEPS
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DWZ
1999-11-05
ULTRA-CBX
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DWZ
1997-12-16
HEARTPORT ENDOAORTIC CLAMP CATHETER
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DWZ
1997-12-16
T-REX BIOPSY FORCEPS
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DWZ
1995-07-27
DYNABITE CARDIOVASCULAR BIOPSY FORCEPS
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DWZ
1994-01-06
CORDIS BIPAL 7 /BIOPSY & BIPAL BIOPSY FORCEPS, MODIF
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DWZ
1993-09-01
CORDIS BIPAL 7 BIOPSY FORCEPS WITH A INLINE HANDLE
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DWZ
1992-10-21
BIOPSY FORCEPS
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DWZ
1992-03-30
CORDIS BIPAL 7 BIOPSY FORCEPS
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DWZ
1991-12-18
CORDIS BIPAL BIOPSY FORCEPS
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DWZ
1991-07-15
VASCULAR BIOPSY FORCEPS
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DWZ
1990-06-29
BIOPSY FORCEPS
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DWZ
1989-10-30
BIOPSY FORCEPS
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DWZ
1989-03-31
REUSABLE MLYOCARDIAL BIOPSY FORCEPS (BIOPTOMES
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DWZ
1988-12-05
FLEXIBLE MYOCARDIAL BIOPSY FORCEPS
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DWZ
1988-11-28
MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES
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DWZ
1988-09-08
MYOCARD BIOPSY FORCEP
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DWZ
1987-02-20
ENDOMYOCARDIAL BIOPSY DEVICE
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DWZ
1981-04-17
CORDIS BIOPSY FORCEPS
View details →No matching devices.
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