Alto Development Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alto Development Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Alto Development Corp. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1982 to 1996.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alto Development Corp.
10 devices
Cleared
Dec 20, 1996
A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON
General & Plastic Surgery
32d
Cleared
Jan 07, 1994
LABELING FOR MYO/WIRE II STERNOTOMY SUTURES
General & Plastic Surgery
227d
Cleared
Sep 07, 1993
A&E MEDICAL ELECTROSURG ELECTRO W/NON-STICK COAT
General & Plastic Surgery
162d
Cleared
May 17, 1993
A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS
General & Plastic Surgery
104d
Cleared
Oct 05, 1992
A&E MEDICAL CORP DISPOS SUCT COAG W/NON STICK COAT
General & Plastic Surgery
383d
Cleared
Feb 18, 1992
A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES
General & Plastic Surgery
89d
Cleared
Nov 30, 1988
RANEY CLIP
General & Plastic Surgery
15d
Cleared
Apr 21, 1988
ELECTRO-CAUTERY SUCTION TUBE
General & Plastic Surgery
17d
Cleared
Aug 12, 1983
PRESSURE MONITORING IV BOTTLE CAP
Cardiovascular
63d
Cleared
Jul 08, 1982
MYO/CLIP
Cardiovascular
48d