HDP — Elevator, Uterine Class II

FDA Device Classification

FDA product code HDP covers "Elevator, Uterine", a Class II medical device regulated under 21 CFR 884.4530. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification details

Product Code
HDP
Device Class
Class II
Regulation Number
884.4530
Submission Type
510(k)
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) clearances

K-NumberApplicantDevice NameDate
K974801Conkin Surgical InstrumentsSINGLE CHANNEL BALLOON CANNULAJul 9, 1998
K974563Clinical InnovationsCOLPO CUP CVC-2000Mar 2, 1998
K882054Zinnanti Surgical InstrumentsHYSTERO KITSep 29, 1988
K820672Bivona Medical TechnologiesHASSON BUEC-3Jul 30, 1982

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.