Reed Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reed Products, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Reed Products, Inc. has 4 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 4 cleared submissions from 1984 to 1984. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Reed Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Reed Products, Inc.
4 devices
Cleared
Aug 14, 1984
FIRST RESPONSE EMERG. MEDICSL - BURNS
General & Plastic Surgery
99d
Cleared
Jul 23, 1984
FIRST RESPONSE EMERG. MEDICAL SYSTEM
General & Plastic Surgery
77d
Cleared
Jul 23, 1984
FIRST RESPONSE EMERG. MEDICAL SYS BONES
General & Plastic Surgery
77d
Cleared
Jul 23, 1984
FIRST RESPONSE EMERG. EYE INJURIES
General & Plastic Surgery
77d