FDA 510(k)

CILCO ASCAN

K-Number: K827371 · 1982-07-09

Decision Date1982-07-09

Product Code

DecisionSubstantially Equivalent

Device Summary

CILCO ASCAN is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1982-07-09 under 510(k) number K827371. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CILCO ASCAN?

CILCO ASCAN is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is Cilco, Inc.. The 510(k) number is K827371.

When did CILCO ASCAN receive FDA 510(k) clearance?

CILCO ASCAN received FDA 510(k) clearance on 1982-07-09, under 510(k) number K827371.

Who is the listed applicant for CILCO ASCAN?

The FDA 510(k) record lists Cilco, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Cilco, Inc. as applicant

K861334CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE K854969CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)K844249K-SOL K843319CILCO I/A SURGICAL PACK K843992CILCOR OPHTHALMIC INSTRUMENTS K843447CILCO DIAMOND KNIFE

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.