Sampler, Amniotic Fluid (Amniocentesis Tray)
FDA product code HIO · 20 cleared devices
Class 1
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.1550
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1976-12-17 – 1996-03-14
HIO
1996-03-14
HIO
1996-03-12
RNS STERILE, DISPOSABLE AMNIOCENTESIS TRAY
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HIO
1993-09-01
AMNIOTEST(TM)
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HIO
1992-11-05
VARIOUS CAMEO MED AMNIOCENTESIS TRAYS, DISPOSABLE
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HIO
1992-04-27
SONO-VU US(TM), MODIFICATION
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HIO
1992-03-30
MEGA AMNIOCENTESIS KIT
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HIO
1991-06-24
SONO-VU US(TM)
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HIO
1990-07-25
ISOFLO(TM) AMNIOCENTESIS TRAY
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HIO
1990-03-29
PERCU-SET(TM)
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HIO
1990-01-12
AMNIOTIC FLUID SAMPLER (AMNIOCENTESIS TRAY)
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HIO
1989-08-04
PHARMASEAL GENETIC AMNIOCENTESIS TRAY
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HIO
1989-07-14
ECHO-TIP DISPOSABLE AMNIOCENTESIS NEEDLE
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HIO
1989-04-07
ULTRASOUND PROCEDURE TRAY AMNICENTESIS TRAY
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HIO
1986-07-07
NEEDLE FOR AMNIOCENTESIS AND CYST PUNCTURE
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HIO
1986-03-17
HURWITZ AMNIOCENTESIS NEEDLE
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HIO
1985-05-22
PMS AMNIOCENTESIS TRAY/KIT
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HIO
1985-01-31
UMI AMNIOCENTESIS KIT W/SPINAL NEEDLE
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HIO
1983-01-18
AMNIO CENTESES KIT W/NEEDLE
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HIO
1980-11-26
APTEK ULTRASOUND PROCEDURE TRAY
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HIO
1976-12-17
AMMOCENTESIS TRAY (KIT)
View details →No matching devices.
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