PGK
2006-06-29
Cannula, Injector, Uterine, Endometrial Biopsy
FDA product code PGK · 1 cleared devices
Class 2
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.4530
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2006-06-29 – 2006-06-29
to deliver saline and/or contrast media to complete saline infusion sonohysterography and/or hysterosalpingogram respectively and to obtain endometrial biopsy
No matching devices.
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