FDA 510(k)

LCL 8

K-Number: K930116 · 1993-06-17

Decision Date1993-06-17

Product CodeEMA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

LCL 8 is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 1993-06-17 under 510(k) number K930116. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LCL 8?

LCL 8 is a medical device that received FDA 510(k) clearance on 1993-06-17. The listed applicant is Voco GmbH. The 510(k) number is K930116.

When did LCL 8 receive FDA 510(k) clearance?

LCL 8 received FDA 510(k) clearance on 1993-06-17, under 510(k) number K930116.

Who is the listed applicant for LCL 8?

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

What is the FDA product code for LCL 8?

The FDA product code for LCL 8 is EMA.

Other records listing Voco GmbH as applicant

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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.