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FDA 510(k)

CAST TOE COVER

K-Number: K823819 · 1983-01-14

ApplicantDanek Medical, Inc.
Decision Date1983-01-14
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CAST TOE COVER is the device name listed in this FDA 510(k) record. The listed applicant is Danek Medical, Inc.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K823819. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAST TOE COVER?

CAST TOE COVER is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Danek Medical, Inc.. The 510(k) number is K823819.

When did CAST TOE COVER receive FDA 510(k) clearance?

CAST TOE COVER received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823819.

Who is the listed applicant for CAST TOE COVER?

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

What is the FDA product code for CAST TOE COVER?

The FDA product code for CAST TOE COVER is LGF.

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Related Devices (Code: LGF)

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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.

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