BARTELS EXTRACELLULAR MATRIX— 510(k) K902726

Name: FDA 510(k) clearance K902726
Creator: U.S. Food and Drug Administration
Published: 1990-09-24

Substantially Equivalent

Baxter Healthcare Corp

FDA 510(k) clearance K902726 for BARTELS EXTRACELLULAR MATRIX, Substantially Equivalent on 1990-09-24. Applicant: Baxter Healthcare Corp. Device class: 1.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code KIR
Device class: Class 1
Regulation: 21 CFR 864.2280
Advisory panel: Hematology
Date received: 1990-06-21
Decision date: 1990-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bellevue, WA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIR

view all

K973209 — FRESH CELLS VERO1997-09-25
K973210 — FRESH CELLS NCI H2921997-09-25
K973211 — FRESH CELLS MV1LU1997-09-25
K973212 — FRESH CELLS WI-381997-09-25
K973213 — FRESH CELLS LLC-MK21997-09-25

More clearances from Baxter Healthcare Corp

view all

K190910 — PrisMax System Version 22019-07-25
K163530 — PrisMax Control Unit2017-05-03
K130531 — ULTRAFUSE2014-04-08
K132734 — NEUTRAL LUER ACTIVATED DEVICE (ONE-LINK NEEDLE-FREE IV CONNECTOR) AND EXTENSION SETS2013-10-08
K130245 — LARGE BORE STOPCOCK WITH ROTATING MALE LUER LOCK/LARGE BORE STOPCOCK WITH EXTENSION SET, GANG LARGE BORE STOPCOCK MANIFO2013-03-01

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