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FDA 510(k)

EOL, MODEL LIO

K-Number: K881984 · 1988-09-06

ApplicantEol, Inc.
Decision Date1988-09-06
Product CodeHLI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EOL, MODEL LIO is the device name listed in this FDA 510(k) record. The listed applicant is Eol, Inc.. It received FDA 510(k) clearance on 1988-09-06 under 510(k) number K881984. The device is classified under product code HLI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EOL, MODEL LIO?

EOL, MODEL LIO is a medical device that received FDA 510(k) clearance on 1988-09-06. The listed applicant is Eol, Inc.. The 510(k) number is K881984.

When did EOL, MODEL LIO receive FDA 510(k) clearance?

EOL, MODEL LIO received FDA 510(k) clearance on 1988-09-06, under 510(k) number K881984.

Who is the listed applicant for EOL, MODEL LIO?

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

What is the FDA product code for EOL, MODEL LIO?

The FDA product code for EOL, MODEL LIO is HLI.

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Official Source

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

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