UTERINE CURETTE— 510(k) K890384

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890384 for UTERINE CURETTE, Substantially Equivalent on 1989-02-13. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code HCY
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1989-01-23
Decision date: 1989-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HCY

K980096 — OAC (OPTICAL ASPIRATING CURETTE)1998-05-01
K944238 — ENDOCYTE TM1995-09-15
K935822 — PHASE I CURETTE1994-04-28
K901442 — BAXTER D & C TRAY1990-07-26
K881794 — IVORY FINDER SET1988-07-08

More clearances from Kinetic Medical Products

K890385 — MIDWIFERY/OBSTETRICAL FORCEPS1989-03-01
K890376 — VAGINAL SPECULUM1989-02-27
K890380 — CERVICAL BIOPSY FORCEPS1989-02-27
K890382 — COMPRESSION FORCEPS1989-02-27
K890387 — MALLEABLE PLACENTA CURETTE1989-02-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.