ELLIK EVACUATOR— 510(k) K791306

Substantially Equivalent

Davol, Inc.

FDA 510(k) clearance K791306 for ELLIK EVACUATOR, Substantially Equivalent on 1979-08-03. Applicant: Davol, Inc.. Device class: 2.

Clearance details

Applicant: Davol, Inc.
Product code: Code KQT
Device class: Class 2
Regulation: 21 CFR 876.4370
Advisory panel: Gastroenterology, Urology
Date received: 1979-07-16
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQT

K964111 — LITHOVAC SUCTION/ASPIRATION PROBE1996-12-16
K921088 — EVACUATOR, GASTRO-UROLOGY1992-10-28
K921451 — EVACUATOR, GASTRO-UROLOGY1992-10-28
K910728 — CLEANFLOW SYSTEM1991-04-01
K880099 — VAN-TEC BLADDER EVACUATOR1988-03-02

More clearances from Davol, Inc.

K251557 — Bard® Mesh; Bard® Mesh Pre-Shaped2025-06-12
K250098 — Bard Soft Mesh; Bard Soft Mesh Pre-Shaped2025-04-09
K031213 — AQUASENS FLUID MONITORING SYSTEM2003-04-30
K030307 — DAVOL ARTHROVENT OUTFLOW TUBING2003-02-13
K003323 — COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,00102052001-01-22

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