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FDA 510(k)

CAUSSE MODIFIED TEFLON PISTON, OTOLOGY

K-Number: K760437 · 1976-10-05

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

Device Summary

CAUSSE MODIFIED TEFLON PISTON, 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 K760437. 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 CAUSSE MODIFIED TEFLON PISTON, OTOLOGY?

CAUSSE MODIFIED TEFLON PISTON, 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 K760437.

When did CAUSSE MODIFIED TEFLON PISTON, OTOLOGY receive FDA 510(k) clearance?

CAUSSE MODIFIED TEFLON PISTON, OTOLOGY received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760437.

Who is the listed applicant for CAUSSE MODIFIED TEFLON PISTON, 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 CAUSSE MODIFIED TEFLON PISTON, OTOLOGY?

The FDA product code for CAUSSE MODIFIED TEFLON PISTON, OTOLOGY is ETB.

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Related Devices (Code: ETB)

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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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