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FDA 510(k)

ENDO-GUARD

K-Number: K830781 · 1983-03-31

ApplicantJayco Pharmaceuticals
Decision Date1983-03-31
Product CodeFOG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ENDO-GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Jayco Pharmaceuticals. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K830781. The device is classified under product code FOG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-GUARD?

ENDO-GUARD is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Jayco Pharmaceuticals. The 510(k) number is K830781.

When did ENDO-GUARD receive FDA 510(k) clearance?

ENDO-GUARD received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830781.

Who is the listed applicant for ENDO-GUARD?

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

What is the FDA product code for ENDO-GUARD?

The FDA product code for ENDO-GUARD is FOG.

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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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