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FDA 510(k)

PLY LESIVE

K-Number: K801047 · 1980-05-20

ApplicantMay-Pell Chemical Development Co.
Decision Date1980-05-20
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLY LESIVE is the device name listed in this FDA 510(k) record. The listed applicant is May-Pell Chemical Development Co.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K801047. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLY LESIVE?

PLY LESIVE is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is May-Pell Chemical Development Co.. The 510(k) number is K801047.

When did PLY LESIVE receive FDA 510(k) clearance?

PLY LESIVE received FDA 510(k) clearance on 1980-05-20, under 510(k) number K801047.

Who is the listed applicant for PLY LESIVE?

The FDA 510(k) record lists May-Pell Chemical Development Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLY LESIVE?

The FDA product code for PLY LESIVE is LBH.

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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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