Holl Meditronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Holl Meditronics, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Holl Meditronics, Inc. has 6 FDA 510(k) cleared medical devices. Based in Collingswood, US.
Historical record: 6 cleared submissions from 1989 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Holl Meditronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Holl Meditronics, Inc.
6 devices
Cleared
Apr 30, 1996
ARCO-MBC, ARCO MC
General & Plastic Surgery
238d
Cleared
Nov 09, 1994
SONOCA III
General & Plastic Surgery
203d
Cleared
Jul 09, 1991
ILCO INFRARED LIGHT COAGULATOR
Gastroenterology & Urology
90d
Cleared
Nov 27, 1990
MOTO-MED RF-II AND PICO
Physical Medicine
545d
Cleared
Jul 03, 1990
SONOCA II ULTRASONIC SURGICAL DEVICE
General & Plastic Surgery
77d
Cleared
Nov 14, 1989
SONOCA ULTRASONIC SURGICAL SYSTEM
General & Plastic Surgery
167d