FDA 510(k)

LEGREST, ELEVATING

K-Number: K780192 · 1978-02-14

Decision Date1978-02-14

Product CodeKNN

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

LEGREST, ELEVATING is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-02-14 under 510(k) number K780192. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEGREST, ELEVATING?

LEGREST, ELEVATING is a medical device that received FDA 510(k) clearance on 1978-02-14. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K780192.

When did LEGREST, ELEVATING receive FDA 510(k) clearance?

LEGREST, ELEVATING received FDA 510(k) clearance on 1978-02-14, under 510(k) number K780192.

Who is the listed applicant for LEGREST, ELEVATING?

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

What is the FDA product code for LEGREST, ELEVATING?

The FDA product code for LEGREST, ELEVATING is KNN.

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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.