Thomas Industries is one of 6981 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thomas Industries - FDA 510(k) Cleared Devices
Recent clearances: CPI, MAXI-VAC(6480),THOMAS INDUSTRIES, MEDI-PUMP(1240/1242/1243)
9
Total
9
Cleared
0
Denied
Thomas Industries has 9 FDA 510(k) cleared medical devices. Based in Sheboygan, US.
Historical record: 9 cleared submissions from 1994 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Thomas Industries Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thomas Industries
9 devices
Cleared
Jun 01, 2004
MEDI-PUMP ASPIRATOR, MODEL 1615
General & Plastic Surgery
25d
Cleared
Mar 04, 1997
CPI, MAXI-VAC(6480),THOMAS INDUSTRIES, MEDI-PUMP(1240/1242/1243)
General & Plastic Surgery
76d
Cleared
Oct 26, 1995
MEDI PUMP ASPIRATOR MODELS 1130 AND 1135
General & Plastic Surgery
129d
Cleared
Aug 24, 1995
MEDI - PUMP
Anesthesiology
211d
Cleared
Aug 21, 1995
MEDI - PUMP
General & Plastic Surgery
129d
Cleared
Apr 19, 1995
MEDI - PUMP
Anesthesiology
51d
Cleared
Jan 18, 1995
MEDI-PUMP
General & Plastic Surgery
132d
Cleared
May 27, 1994
NEBULIZER PUMP, POWERED, MODEL 1110
Anesthesiology
602d
Cleared
Jan 12, 1994
NEBULIZER PUMP, POWERED MODEL 1180
Anesthesiology
467d