System, Abortion, Vacuum
FDA product code HHI · 24 cleared devices
Class 2
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.5070
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1978-04-12 – 2017-09-29
HHI
2017-09-29
HHI
2003-06-23
BERKELEY V-10 VACUUM CURETTAGE SYSTEM
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HHI
1998-11-16
CYTOPREP
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HHI
1994-03-15
MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER
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HHI
1990-11-02
CYTOSMEAR BRUSH
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HHI
1990-03-30
CANNULA, SUCTION UTERINE
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HHI
1990-03-19
SWIVEL ADAPTER
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HHI
1988-04-25
SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS
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HHI
1987-11-25
CANNULA AND GENERAL PURPOSE ASPIRATOR
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HHI
1987-03-05
COSMEDTECH GENERAL ASPIRATOR
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HHI
1987-03-04
COSMEDTECH CANNULA
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HHI
1986-07-18
LS3000 CANNULA UTERINE SUCTION
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HHI
1985-02-28
GYNASPYR VACUUM CURETTAGE UNIT
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HHI
1984-07-03
MODEL 3014 SUCTION UNIT
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HHI
1984-04-30
DIAGNOSTIC DILATATION & MENSTRUAL KIT
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HHI
1984-04-30
MENSTRUAL ASPIRATION KIT
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HHI
1984-04-30
VACUUM ASPIRATION CATHETER
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HHI
1984-04-30
TAPERED CERVICAL DILATOR
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HHI
1984-03-30
MEDEVICE V-80 VACUUM PUMP
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HHI
1983-06-30
EPCOM VCU-1 VACUUM SYSTEM & CURETTE
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HHI
1981-12-14
SYNEVAC VACUUM CURETTAGE SYSTEMS
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HHI
1980-10-31
UTERINE VACUM ASPIRATING CURRETTE
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HHI
1980-05-14
VABRA ASPIRATOR
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HHI
1978-04-12
VABRA ABORTION UNIT
View details →No matching devices.
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