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FDA 510(k)

POLY PLUG CEMENT RESTRICTOR

K-Number: K840242 · 1984-05-30

ApplicantLatham Manufacturer
Decision Date1984-05-30
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POLY PLUG CEMENT RESTRICTOR is the device name listed in this FDA 510(k) record. The listed applicant is Latham Manufacturer. It received FDA 510(k) clearance on 1984-05-30 under 510(k) number K840242. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLY PLUG CEMENT RESTRICTOR?

POLY PLUG CEMENT RESTRICTOR is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Latham Manufacturer. The 510(k) number is K840242.

When did POLY PLUG CEMENT RESTRICTOR receive FDA 510(k) clearance?

POLY PLUG CEMENT RESTRICTOR received FDA 510(k) clearance on 1984-05-30, under 510(k) number K840242.

Who is the listed applicant for POLY PLUG CEMENT RESTRICTOR?

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

What is the FDA product code for POLY PLUG CEMENT RESTRICTOR?

The FDA product code for POLY PLUG CEMENT RESTRICTOR is JDS.

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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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