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FDA 510(k)

SHEA TORP, OTOLOGY IMPLANT

K-Number: K760433 · 1976-10-05

Decision Date1976-10-05
Product CodeETA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SHEA TORP, OTOLOGY IMPLANT 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 1976-10-05 under 510(k) number K760433. The device is classified under product code ETA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHEA TORP, OTOLOGY IMPLANT?

SHEA TORP, OTOLOGY IMPLANT is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K760433.

When did SHEA TORP, OTOLOGY IMPLANT receive FDA 510(k) clearance?

SHEA TORP, OTOLOGY IMPLANT received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760433.

Who is the listed applicant for SHEA TORP, OTOLOGY IMPLANT?

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 SHEA TORP, OTOLOGY IMPLANT?

The FDA product code for SHEA TORP, OTOLOGY IMPLANT is ETA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Richard'S Medical Equip., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 48 devices →

Related Devices (Code: ETA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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