TUBING, NONINVASIVE— 510(k) K945978

Name: FDA 510(k) clearance K945978
Creator: U.S. Food and Drug Administration
Published: 1995-01-11

Substantially Equivalent

Endoscopic Technologies, Inc.

FDA 510(k) clearance K945978 for TUBING, NONINVASIVE, Substantially Equivalent on 1995-01-11. Applicant: Endoscopic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Endoscopic Technologies, Inc.
Product code: Code GAZ
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1994-12-08
Decision date: 1995-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norcross, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GAZ

view all

K952605 — SUCTION/IRRIGATOR TUBING KIT1995-09-15
K930512 — SUCTION/IRRIGATION Y TUBING SET W/TRUMPET VALVES1993-07-23
K911865 — NORTEC CONNECTING TUBE SET1991-11-01
K910471 — MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE1991-03-08
K910170 — MAXI-FLOW SUCTION SET 12 FT.1991-02-01

More clearances from Endoscopic Technologies, Inc.

view all

K060101 — ESTECH AORTIC EASY FLOW CANNULA2006-05-10
K053326 — ESTECH COBRA ELECTROSURGICAL UNIT & CABLE2006-01-06
K053100 — ESTECH COBRA BIPOLAR SYSTEM2005-12-19
K946105 — ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES1995-04-06
K945979 — TROCAR/CANNULA1994-12-21

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