Cap, Cervical
FDA product code HDR · 29 cleared devices
Class 2
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.5250
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1981-07-13 – 2025-04-02
HDR
2025-04-02
HDR
2023-06-23
FERTI-LILY Conception Cup
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HDR
2000-03-21
OVES CERVICAL CAP
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HDR
1995-05-15
IMAGYN INTRAUTERINE INSEMINATION DEVICE
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HDR
1995-05-11
COOK INSEMINATION CUP
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HDR
1990-10-05
MINISPACE(TM) IUI CATHETER
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HDR
1990-08-28
COAXIAL CATHETER SET
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HDR
1990-06-26
INTRAUTERINE INSEMINATION CATHETERS
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HDR
1990-04-16
MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPES
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HDR
1990-04-13
SPERM SELECT SYSTEM
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HDR
1990-02-16
DGH A-SAN PROBE HOLDER
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HDR
1989-09-22
MODIFIED HAM'S F-10 W/ALBUMIN
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HDR
1989-09-22
HTF WITH ALBUMIN (CATALOG NO. 9994)
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HDR
1989-08-15
KDF-2.3
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HDR
1989-03-31
SHEPARD INTRAUTERINE INSEMINATION CATHETER
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HDR
1989-01-27
RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET
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HDR
1988-06-14
CERVICATH
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HDR
1988-03-31
SPERM WASHING MEDIUM #9983 & MODIFIED #9984
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HDR
1987-09-28
SPERM-SELECT ADDITIONAL INDICATION
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HDR
1987-08-14
CAT. #9972 REFRIGERATION MEDIUM (TEST YOLK BUFFER)
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HDR
1987-08-14
FREEZING MEDIUM (TEST YOLK BUFFER W/GLYCEROL)
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HDR
1987-07-16
SPERM WASHING MEDIUM #9932
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HDR
1987-07-15
HTF MEDIUM AND MODIFIED HTF MEDIUM-HEPES
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HDR
1987-03-02
INTRAUTERINE INSEMINATION CATHETER
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HDR
1987-01-06
SPERM CAPACITATION MEDIUM
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HDR
1986-12-11
MAKLER CATHETER
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HDR
1986-12-11
INTRAUTERINE CATHETER
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HDR
1983-07-12
AXCAN SPERM CUP
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HDR
1981-07-13
AXISONIC II
View details →No matching devices.
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