Johnson & Johnson Patient Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Johnson & Johnson Patient Care, Inc. - FDA 510(k) Cleared Devices
4
Total
2
Cleared
0
Denied
Johnson & Johnson Patient Care, Inc. has 2 FDA 510(k) cleared medical devices. Based in New Brunswick, US.
Historical record: 2 cleared submissions from 1988 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Johnson & Johnson Patient Care, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Johnson & Johnson Patient Care, Inc.
4 devices
Cleared
Oct 13, 1989
JOHNSON & JOHNSON TUBE SECUREMENT DEVICE
General Hospital
37d
Cleared
Sep 26, 1989
ACTISORB* PLUS ACTIVATED CHARCOAL DRESS W/SILVER
General & Plastic Surgery
161d
Cleared
Mar 23, 1989
NU-DERM HYDROCOLLOID DRESSING
General & Plastic Surgery
48d
Cleared
Dec 15, 1988
JOHNSON & JOHNSON STERILE SPRAY TIP SYRINGE
General Hospital
31d