ACUTE HEMODIALYSIS TRAYS— 510(k) K833139

Substantially Equivalent

Intermed, Inc.

FDA 510(k) clearance K833139 for ACUTE HEMODIALYSIS TRAYS, Substantially Equivalent on 1983-12-22. Applicant: Intermed, Inc.. Device class: 2.

Clearance details

Applicant: Intermed, Inc.
Product code: Code KNZ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1983-09-14
Decision date: 1983-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNZ

K842039 — ARGON DUAL LUMEN HEMODIALYSIS, CATHETER1985-01-29
K844612 — ACUTE HEMODIALYSIS TRAYS1984-12-17
K842864 — VACCESS FEMORAL CANNULA1984-08-08
K842416 — DUO FLOW CATHETER-MC 541984-07-26
K841530 — DOUBLE LUMEN SUBLCAVIAN-FEMORAL1984-06-25

More clearances from Intermed, Inc.

K900857 — NON STERILE PARENTERAL SUPPLY KIT1990-05-22
K842166 — INTERMED, INS STERILE WATER/SALINE1985-02-12
K833126 — DRESSING CHANGE TRAYS1984-01-27
K833573 — CENTRAL VEIN CATH. TRAY CC-20-14201984-01-11
K833574 — PERCUTANEOUS SHEATH INTRODUCER TRAYS1984-01-11

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