Medical Device Manufacturer · US , Mchenry , IL

Cilco, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1982

Total

Cleared

Denied

Cilco, Inc. has 12 FDA 510(k) cleared ophthalmic devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1982 to 1986.

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 - Cilco, Inc.

12 devices

1-12 of 12

Cleared May 02, 1986

CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE

K861334 · HNN

Ophthalmic · 23d

Cleared Feb 27, 1986

CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)

CILCO I/A SURGICAL PACK

K843319 · HQC

Ophthalmic · 174d

Cleared Nov 21, 1984

CILCOR OPHTHALMIC INSTRUMENTS

Cilco, Inc. - FDA 510(k) Cleared Devices

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