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FDA 510(k)

FIGLEAF SHIELD

K-Number: K930763 · 1993-05-17

ApplicantByers Industries, Inc.
Decision Date1993-05-17
Product CodeIWT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FIGLEAF SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Byers Industries, Inc.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K930763. The device is classified under product code IWT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIGLEAF SHIELD?

FIGLEAF SHIELD is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Byers Industries, Inc.. The 510(k) number is K930763.

When did FIGLEAF SHIELD receive FDA 510(k) clearance?

FIGLEAF SHIELD received FDA 510(k) clearance on 1993-05-17, under 510(k) number K930763.

Who is the listed applicant for FIGLEAF SHIELD?

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

What is the FDA product code for FIGLEAF SHIELD?

The FDA product code for FIGLEAF SHIELD is IWT.

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Related Devices (Code: IWT)

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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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