J & B Assoc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
J & B Assoc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
J & B Assoc. has 10 FDA 510(k) cleared ophthalmic devices. Based in Dallas, US.
Historical record: 10 cleared submissions from 1990 to 1990.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - J & B Assoc.
10 devices
Cleared
May 03, 1990
MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS
Ophthalmic
90d
Cleared
May 03, 1990
MODEL N742 SUNGLASSES W/POLYCARBONATE BLUE BLOCKER
Ophthalmic
90d
Cleared
May 03, 1990
MODEL N741 SUNGLASSES W/ACRYLIC BLUE COMPUTER LENS
Ophthalmic
90d
Cleared
May 03, 1990
MODEL F3 FLIP UP SUNGLASSES W/POLORIZED COMPUTER
Ophthalmic
90d
Cleared
May 03, 1990
MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENS
Ophthalmic
90d
Cleared
May 03, 1990
MODEL S139029 SUNGLASSES W/MIRROR ACRYLIC LENSES
Ophthalmic
90d
Cleared
May 03, 1990
MODEL 8806 SD SUNGLASSES W/ACRYLIC LENSES
Ophthalmic
90d
Cleared
May 03, 1990
MODEL 9018 PC SUNGLASSES W/POLYCARBONATE LENSES
Ophthalmic
90d
Cleared
Feb 27, 1990
MODEL F3 FLIP-UP SUNGLASSES W/ACRYLIC ORANGE COMP.
Ophthalmic
25d
Cleared
Feb 27, 1990
MODEL F 1 FLIP-UP SUNGLASSES W/POLYCARBONATE BLUE
Ophthalmic
25d