EMODIALYSIS DEL. SYS. MODEL 7110— 510(k) K771696

Name: FDA 510(k) clearance K771696
Creator: U.S. Food and Drug Administration
Published: 1977-09-15

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K771696 for EMODIALYSIS DEL. SYS. MODEL 7110, Substantially Equivalent on 1977-09-15. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code FKP
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1977-09-06
Decision date: 1977-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FKP

view all

K181991 — NxStage Connected Health System2018-09-26
K131739 — NXSTAGE CONNECTED HEALTH SYSTEM2013-10-10
K130460 — NXSTAGE DOSING CALCULATOR2013-07-11
K040074 — ONEVIEW INTERFACE2004-04-08
K021060 — FRESENIUS ICARE MONITORING SYSTEM2002-11-13

More clearances from Bd Becton Dickinson Vacutainer Systems Preanalytic

view all

K003062 — BACTEC MGIT 960 SIR KITS2001-06-06
K003553 — 0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE2001-03-21
K003461 — BD VACUTAINER PASSIVE SHIELDING BLOOD COLLECTION NEEDLE2001-02-01
K002938 — B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/162000-11-29
K001364 — BD DIRECTIGEN FLU A+B2000-06-28

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