MANIPULATOR & INJECTOR, UTERINE— 510(k) K770727

Name: FDA 510(k) clearance K770727
Creator: U.S. Food and Drug Administration
Published: 1977-04-26

Substantially Equivalent

National Catheter Co. Div. Mallinckrodt

FDA 510(k) clearance K770727 for MANIPULATOR & INJECTOR, UTERINE, Substantially Equivalent on 1977-04-26. Applicant: National Catheter Co. Div. Mallinckrodt. Device class: 2.

Clearance details

Applicant: National Catheter Co. Div. Mallinckrodt
Product code: Code KNA
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1977-04-19
Decision date: 1977-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNA

view all

K130087 — PANPAC WORD/BARTHOLIN CATHETER2014-01-10
K102141 — COOK WORD BARTHOLIN GLAND CATHETER (FINAL TRADE NAME NOT YET DETERMINED)2011-05-06
K093904 — GLENVEIGH VAGINAL TAMPONADE BALLOON CATHETER2010-04-14
K082939 — COOK FETAL MEMBRANE MANIPULATOR, MODEL -FMM-1224002009-09-03
K062438 — BAKRI POSTPARTUM BALLOON, MODEL J-SOS-1005002006-10-27

More clearances from National Catheter Co. Div. Mallinckrodt

view all

K802918 — ANTHRON CATHETER SET1981-04-21
K802505 — DOUBLE LUMEN TRACHEAL TUBE1981-03-13
K810321 — REINFORCED TRACHEOSTOMY TUBE SET(TENTAT)1981-03-04
K801924 — HI-LO TEMP GEN. PURPOSE TEMP. PROBE1980-09-09
K801005 — MLT TUBE MICROLARYNGEAL TRACHEAL TUBE)1980-05-23

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