UTERINE INJECTOR 2MM— 510(k) K873515

Name: FDA 510(k) clearance K873515
Creator: U.S. Food and Drug Administration
Published: 1987-09-29

Substantially Equivalent

Zinnanti Surgical Instruments, Inc.

FDA 510(k) clearance K873515 for UTERINE INJECTOR 2MM, Substantially Equivalent on 1987-09-29. Applicant: Zinnanti Surgical Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Zinnanti Surgical Instruments, Inc.
Product code: Code HES
Device class: Class 2
Regulation: 21 CFR 884.1300
Advisory panel: Obstetrics/Gynecology
Date received: 1987-08-31
Decision date: 1987-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodland Hills, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HES

view all

K140761 — KAHN UTERINE CANNULA, JARCHO UTERINE CANNULA, NEAL FALLOPIAN CANNULA2014-04-21
K000340 — HYSTALOG HSG CATHETER2000-04-19
K903209 — MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER1990-12-21
K903208 — MAXI-FLOW INSUFFLATOR TUBING SET1990-12-17
K904473 — KRONNER MANIPUJECTOR1990-12-14

More clearances from Zinnanti Surgical Instruments, Inc.

view all

K925501 — NYLON COATED SPECULA1997-06-13
K941458 — UTERINE MANIPULATOR/INJECTOR WITH SPRING1995-01-25
K941457 — UTERINE INJECTOR WITH SPRING1995-01-24
K925560 — ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES1994-08-30
K925957 — SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE1994-06-07

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