ClearanceBrief
Company ยท US

MRL, Inc., A Welch Allyn Company

FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2004. Name variants (Inc, Corp, punctuation) are merged.

1510(k) clearances (0 in 12 months)
5recalls (0 in 12 months)
5recalls that name a 510(k)

Product codes

CodeDeviceRecords
MKJAutomated External Defibrillators (Non-Wearable)4
MJKDna Probe, Trichomonas Vaginalis2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 25, 2004K033642SMARTLANK WIRELESS, MODEL 001970
Mrl, A Welch Allyn Company
MKJ

Latest recalls

DateFirm and productCodeLinked 510(k)
Jan 19, 2007MRL, Inc., A Welch Allyn Company
Welch Allyn PIC 50 Portable Intensive Care System, Multi-Parameter Monitor/Defibrillator; a portable 12V internal battery powered defibrillator; Manufactured by MRL Inc., a WelchAllyn Company, 1000 As
Terminated
MJKK974034
Jul 8, 2006MRL, Inc., A Welch Allyn Company
Welch Allyn PIC 50 Portable Intensive Care System Multi-Parameter Monitor/Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, 1000 A
Terminated
MJKK974034
Jun 22, 2006MRL, Inc., A Welch Allyn Company
Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, 1000 Asbury Drive, Buffalo Grove, Illinois
Terminated
MKJK002232
May 12, 2005MRL, Inc., A Welch Allyn Company
Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, 1000 Asbury Drive, Buffalo Grove, Illinois
Terminated
MKJK002232
Jul 20, 2004MRL, Inc., A Welch Allyn Company
Welch Allyn AED 10 Defibrillator; a battery powered automated external defibrillator; Manufacturer: MRL, Inc., A Welch Allyn Company, 100 Asbury Drive, Buffalo Grove, Illinois 60089; Model AED10, part
Terminated
MKJK021168
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