ClearanceBrief
Company ยท US

Continental Medical Laboratories, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1997. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FCMTray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)1
GDTStaple, Removable (Skin)1
JOHTube Tracheostomy And Tube Cuff1
KMFBandage, Liquid1
LROGeneral Surgery Tray1
LYYLatex Patient Examination Glove1
MCYWound Dressing Kit1
MCZSuture Removal Kit1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 14, 1997K964827PROD. NO. 01-132 - SUTURE REMOVAL KIT
Continental Medical Laboratories, Inc.
MCZ
Oct 21, 1996K963234STAPLE REMOVAL KIT
Continental Medical Laboratories, Inc.
GDT
Oct 17, 1996K963443PROD. NO. 02-031 - LACERATION TRAY
Continental Medical Laboratories, Inc.
LRO
Oct 11, 1996K962078TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER
Continental Medical Laboratories, Inc.
JOH
Sep 23, 1996K954728PROD NO. 01-1694 - 4X4 FOAM DRESSING
Continental Medical Laboratories, Inc.
KMF
Jun 21, 1996K962073URETHRAL CATHETERIZATION TRAY/UNIVERSAL URETHRAL CATH TRAY
Continental Medical Laboratories, Inc.
FCM
Jun 14, 1995K952335WOUND CARE MANAGEMENT KITS
Continental Medical Laboratories, Inc.
LYY
Mar 27, 1991K905123G-TUBE DRESSING CHANGE TRAY
Continental Medical Laboratories, Inc.
MCY

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes