American Surgical Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Surgical Co., Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
American Surgical Co., Inc. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 9 cleared submissions from 1983 to 1986. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by American Surgical Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Surgical Co., Inc.
9 devices
Cleared
Feb 07, 1986
VITREONIC PLUS
Ophthalmic
847d
Cleared
Feb 07, 1986
VIT PAC
Ophthalmic
847d
Cleared
Oct 05, 1984
AMER. SURGICAL CORP. EXTRA PLUS PAK
Ophthalmic
161d
Cleared
Dec 28, 1983
EXTRA PLUS TM
Ophthalmic
75d
Cleared
Dec 28, 1983
EXTRA SENSORY PAK-DISPOS. ACCESS
Ophthalmic
71d
Cleared
Dec 28, 1983
EXTRA SENSORY PLUS
Ophthalmic
75d
Cleared
Dec 28, 1983
PHACOTRON PLUS
Ophthalmic
75d
Cleared
Dec 28, 1983
UNIVERSAL PAC
Ophthalmic
75d
Cleared
Dec 28, 1983
ULTRAVIT
Ophthalmic
75d