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FDA 510(k)

AUDIOTECH MODEL DP

K-Number: K931975 · 1993-06-22

ApplicantMuskogee Regional Hearing Aid Lab
Decision Date1993-06-22
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AUDIOTECH MODEL DP is the device name listed in this FDA 510(k) record. The listed applicant is Muskogee Regional Hearing Aid Lab. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K931975. 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 AUDIOTECH MODEL DP?

AUDIOTECH MODEL DP is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Muskogee Regional Hearing Aid Lab. The 510(k) number is K931975.

When did AUDIOTECH MODEL DP receive FDA 510(k) clearance?

AUDIOTECH MODEL DP received FDA 510(k) clearance on 1993-06-22, under 510(k) number K931975.

Who is the listed applicant for AUDIOTECH MODEL DP?

The FDA 510(k) record lists Muskogee Regional Hearing Aid Lab as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUDIOTECH MODEL DP?

The FDA product code for AUDIOTECH MODEL DP 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 Muskogee Regional Hearing Aid Lab 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.

K950963AUDIOTECH MODEL SPIK903479AUDIOTECH MODEL DBK903478AUDIOTECH MODEL CL

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.

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