Medical Device Manufacturer · US , Columbus , IN

Applied Laboratories, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1985

Total

Cleared

Denied

Applied Laboratories, Inc. has 9 FDA 510(k) cleared medical devices. Based in Columbus, US.

Historical record: 9 cleared submissions from 1985 to 1988. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Applied Laboratories, Inc. Filter by specialty or product code using the sidebar.

Applied Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Applied Laboratories, Inc.

9 devices

1-9 of 9

Cleared Mar 24, 1988

MOBAY (BAYER) MAKROLON 2658 1112

MOBAY (BAYER) MERLON M-40 (H)F 1112

K873822 · LRX

Ophthalmic · 185d

Cleared Mar 24, 1988

MOBAY (BAYER) MAKROLON 2658 3291

K873823 · LRX

Ophthalmic · 185d

Cleared Mar 24, 1988

RED #467, #457, BLUE #437, GREEN #447 MINDEL S1000

KESTREL CONTACT LENS CASE

K871714 · LPN

Ophthalmic · 22d

Cleared May 29, 1986

EASY EYES TM LENS CARRYING CASE

K860677 · HPX

Ophthalmic · 93d

Cleared Dec 10, 1985

EASY EYES TM LENS CARRYING CASE

K853870 · HPX

Ophthalmic · 84d

Applied Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Applied Laboratories, Inc.

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