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FDA 510(k)

TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY

K-Number: K760434 · 1976-10-05

ApplicantRichard'S Medical Equip., Inc.
Decision Date1976-10-05
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY 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 K760434. The device is classified under product code ETB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY?

TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY 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 K760434.

When did TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY receive FDA 510(k) clearance?

TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760434.

Who is the listed applicant for TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY?

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 TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY?

The FDA product code for TRAPEZE PLATINUM RIBBON LOOP, OTOLOGY is ETB.

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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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