Emerson-Sack-Warner Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Emerson-Sack-Warner Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Emerson-Sack-Warner Corp. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1982 to 1982. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Emerson-Sack-Warner Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Emerson-Sack-Warner Corp.
4 devices
Cleared
Jul 30, 1982
STAND, SURG. INSTRUMENT & DRESSING
General & Plastic Surgery
31d
Cleared
Jul 30, 1982
TABLE, SURG. INSTRUMENT & DRESSING
General & Plastic Surgery
31d
Cleared
Jul 13, 1982
TABLE, OPERATING, FIELD 6530-00-709-8175
General & Plastic Surgery
14d
Cleared
Jul 13, 1982
TABLE, OPERATING, FIELD 6530-00-709-8155
General & Plastic Surgery
14d