Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MERIDIAN DSP

K-Number: K972431 · 1997-07-23

ApplicantMicro-Ear Technology, Inc.
Decision Date1997-07-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MERIDIAN DSP is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Ear Technology, Inc.. It received FDA 510(k) clearance on 1997-07-23 under 510(k) number K972431. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIDIAN DSP?

MERIDIAN DSP is a medical device that received FDA 510(k) clearance on 1997-07-23. The listed applicant is Micro-Ear Technology, Inc.. The 510(k) number is K972431.

When did MERIDIAN DSP receive FDA 510(k) clearance?

MERIDIAN DSP received FDA 510(k) clearance on 1997-07-23, under 510(k) number K972431.

Who is the listed applicant for MERIDIAN DSP?

The FDA 510(k) record lists Micro-Ear Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERIDIAN DSP?

The FDA product code for MERIDIAN DSP is ESD.

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 Micro-Ear Technology, 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.

K041302REFUGE SOUND GENERATORK970880POWER D, TRU 5, PERSONA, PERSONA CHOICE, MERIDIANK964657SUPER K-AMP, EZ-COMPRESSION, TRIM-PRO, HF-PRO, ENVIRO-PRO, COMPRESSION-PRO, COMPRESSION 3000, HF 3000, OCTIVA, REFLEX HFK934149MICRO-TECH TRU CANAL

Related Devices (Code: ESD)

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.

K232999Lyric4 Hearing AidSonova AGK130790LYRIC2Phonak, LLCK081136LYRIC HEARING AIDInsound Medical, Inc.K021867INSOUND XT SERIES HEARING AIDInsound Medical, Inc.K003558TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)Siemens Hearing Instruments, Inc.K984518SONIC INNOVATIONS COMPLETELY-IN-THE-CANAL DSP HEARING AID WITH SOFT SHELLSonic Innovations, 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.

↑