Mcneil-Ppc, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mcneil-Ppc, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Mcneil-Ppc, Inc. has 6 FDA 510(k) cleared medical devices. Based in Skillman, US.
Historical record: 6 cleared submissions from 2002 to 2008. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Mcneil-Ppc, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mcneil-Ppc, Inc.
6 devices
Cleared
Sep 25, 2008
K-Y BRAND INTRIGUE 2-IN-1 MASSAGE CREME
Obstetrics & Gynecology
147d
Cleared
Mar 06, 2008
K-Y BRAND YOURS+MINE
Obstetrics & Gynecology
191d
Cleared
Dec 12, 2007
K-Y BRAND INTRIGUE INTENSE WARMING SENSATION
Obstetrics & Gynecology
112d
Cleared
Jan 26, 2007
K-Y BRAND TOUCH MASSAGE 2-IN-1 TINGLING
Obstetrics & Gynecology
150d
Cleared
Feb 17, 2006
K-Y BRAND SENSUAL MIST
Obstetrics & Gynecology
73d
Cleared
Dec 06, 2002
O.B. TAMPONS
Obstetrics & Gynecology
23d