Solco Basle, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solco Basle, Inc. - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Solco Basle, Inc. has 9 FDA 510(k) cleared anesthesiology devices. Based in Walker, US.
Historical record: 9 cleared submissions from 1985 to 1993.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Solco Basle, Inc.
10 devices
Cleared
Feb 25, 1993
SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEM
Anesthesiology
589d
Cleared
Feb 25, 1993
SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEM
Anesthesiology
584d
Cleared
Aug 14, 1992
SOLCOVAC WOUND DRAINAGE SYSTEM
General & Plastic Surgery
227d
Cleared
Apr 05, 1990
SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEM
Anesthesiology
121d
Cleared
Apr 05, 1990
SOLCOTRANS INTRAOPERATIVE AUTOTRANSFUSION SYSTEM
Anesthesiology
121d
Cleared
Feb 01, 1990
SOLCOSEPT(TM) BLOOD TRANSFUSION FILTER
General Hospital
98d
Cleared
Oct 28, 1988
SOLCOTRANS ORTHO. DRAINAGE/REINFUSION SYSTEM
Anesthesiology
101d
Cleared
Sep 04, 1987
SOLCOTRANS CHEST DRAINAGE AUTOTRANSFUSION SYSTEM
Anesthesiology
65d
Cleared
Jul 07, 1987
HALL VEIN STRIPPER
Cardiovascular
33d
Cleared
Oct 01, 1985
SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS
Anesthesiology
368d