FDA 510(k)

HIP PLATE REMOVAL INSTRUMENT

K-Number: K780300 · 1978-02-28

Decision Date1978-02-28

Product CodeHWB

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

HIP PLATE REMOVAL INSTRUMENT 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 1978-02-28 under 510(k) number K780300. The device is classified under product code HWB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIP PLATE REMOVAL INSTRUMENT?

HIP PLATE REMOVAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1978-02-28. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K780300.

When did HIP PLATE REMOVAL INSTRUMENT receive FDA 510(k) clearance?

HIP PLATE REMOVAL INSTRUMENT received FDA 510(k) clearance on 1978-02-28, under 510(k) number K780300.

Who is the listed applicant for HIP PLATE REMOVAL INSTRUMENT?

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 HIP PLATE REMOVAL INSTRUMENT?

The FDA product code for HIP PLATE REMOVAL INSTRUMENT is HWB.

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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.