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FDA 510(k)

PLUG-LOK CEMENT RESTIRCTOR

K-Number: K791125 · 1979-06-27

ApplicantRichard'S Medical Equip., Inc.
Decision Date1979-06-27
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PLUG-LOK CEMENT RESTIRCTOR is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K791125. The device is classified under product code LZN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLUG-LOK CEMENT RESTIRCTOR?

PLUG-LOK CEMENT RESTIRCTOR is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K791125.

When did PLUG-LOK CEMENT RESTIRCTOR receive FDA 510(k) clearance?

PLUG-LOK CEMENT RESTIRCTOR received FDA 510(k) clearance on 1979-06-27, under 510(k) number K791125.

Who is the listed applicant for PLUG-LOK CEMENT RESTIRCTOR?

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

What is the FDA product code for PLUG-LOK CEMENT RESTIRCTOR?

The FDA product code for PLUG-LOK CEMENT RESTIRCTOR is LZN.

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Related Devices (Code: LZN)

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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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