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FDA 510(k)

OLYMPIA FACEPLATE MODULE

K-Number: K896304 · 1990-01-26

ApplicantOlympia Instruments, Inc.
Decision Date1990-01-26
Product CodeLRB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

OLYMPIA FACEPLATE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Olympia Instruments, Inc.. It received FDA 510(k) clearance on 1990-01-26 under 510(k) number K896304. The device is classified under product code LRB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPIA FACEPLATE MODULE?

OLYMPIA FACEPLATE MODULE is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Olympia Instruments, Inc.. The 510(k) number is K896304.

When did OLYMPIA FACEPLATE MODULE receive FDA 510(k) clearance?

OLYMPIA FACEPLATE MODULE received FDA 510(k) clearance on 1990-01-26, under 510(k) number K896304.

Who is the listed applicant for OLYMPIA FACEPLATE MODULE?

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

What is the FDA product code for OLYMPIA FACEPLATE MODULE?

The FDA product code for OLYMPIA FACEPLATE MODULE is LRB.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Olympia Instruments, 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.

K852244HEARING AID(ALL IN EAR)

Related Devices (Code: LRB)

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.

K974219FACEPLATE ASSEMBLYFinetone Hearing InstrumentsK961593INTRASTAR PRE-WIRED FACEPLATE FOR IN-THE-EAR HEARING AIDSSegi Hearing Aid Co.K942722MODULE PROGRAMElectone, Inc.K942236AUDINA PREWIRES (FACEPLATE HEARING AID SERIES)Audina Hearing InstrumentK935048ARTISAN PROGRAMMER & HEARING AIDTelex Communications, Inc.K933046SILVER L MODULE, ITEElectone, Inc.

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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