ELLIK BLADDER EVACUATOR— 510(k) K800397

Substantially Equivalent

Sage Products, Inc.

FDA 510(k) clearance K800397 for ELLIK BLADDER EVACUATOR, Substantially Equivalent on 1980-03-10. Applicant: Sage Products, Inc.. Device class: 2.

Clearance details

Applicant: Sage Products, Inc.
Product code: Code KQT
Device class: Class 2
Regulation: 21 CFR 876.4370
Advisory panel: Gastroenterology, Urology
Date received: 1980-02-26
Decision date: 1980-03-10
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 Sage Products, Inc.

K972705 — RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTIC1998-04-30
K980490 — SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPS1998-02-24
K973911 — 2 GALLON ALTERNATE CARE SHARPS CONTAINER1997-10-29
K972279 — SHARPS SHUTTLE1997-08-29
K970135 — NITRILE GLOVES1997-08-25

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