FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

UTERINE TENTACULUM

K Number: K890379 · Decision Feb 13, 1989
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
19
Applicant Total
63
Review Days
21

Basic Information

Device Name
UTERINE TENTACULUM
K Number
K890379
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
KINETIC MEDICAL PRODUCTS
Date Received
January 23, 1989
Decision Date
February 13, 1989
Product Code
HDC
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HDC Tenaculum, Uterine

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HDC), ordered by most recent decision date.

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Other Clearances by KINETIC MEDICAL PRODUCTS

K Number Device Name
K890385 MIDWIFERY/OBSTETRICAL FORCEPS
K890382 COMPRESSION FORCEPS
K890387 MALLEABLE PLACENTA CURETTE
K890376 VAGINAL SPECULUM
K890380 CERVICAL BIOPSY FORCEPS
K890383 HYSTERECTOMY FORCEPS
K890216 MICROSURGICAL KERATOME
K890375 VAGINAL SPECULUM
K890377 FIXED-SIZE UTERINE DILATOR
K890389 UMBILICAL SCISSORS
Search all 63 clearances from KINETIC MEDICAL PRODUCTS →