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FDA 510(k)

SHIELD

K-Number: K780263 · 1978-05-03

ApplicantLorvic Corp.
Decision Date1978-05-03
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Lorvic Corp.. It received FDA 510(k) clearance on 1978-05-03 under 510(k) number K780263. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHIELD?

SHIELD is a medical device that received FDA 510(k) clearance on 1978-05-03. The listed applicant is Lorvic Corp.. The 510(k) number is K780263.

When did SHIELD receive FDA 510(k) clearance?

SHIELD received FDA 510(k) clearance on 1978-05-03, under 510(k) number K780263.

Who is the listed applicant for SHIELD?

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

What is the FDA product code for SHIELD?

The FDA product code for SHIELD is EJK.

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Other records listing Lorvic Corp. as applicant

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Related Devices (Code: EJK)

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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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