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)

MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID

K-Number: K931035 · 1993-06-01

ApplicantMaico Hearing Instruments, Inc.
Decision Date1993-06-01
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Maico Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1993-06-01 under 510(k) number K931035. 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 MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID?

MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID is a medical device that received FDA 510(k) clearance on 1993-06-01. The listed applicant is Maico Hearing Instruments, Inc.. The 510(k) number is K931035.

When did MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID receive FDA 510(k) clearance?

MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID received FDA 510(k) clearance on 1993-06-01, under 510(k) number K931035.

Who is the listed applicant for MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID?

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

What is the FDA product code for MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID?

The FDA product code for MODELS 33PP, 33PP ANR, & 33PP SUPER HEARING AID 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 Maico Hearing 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.

K960031AUDIOFLEX 120K954054MAICO PRODIGY CIC SERIESK953161MAICO MA630D AUDIOMETER WITH OPTIONAL REFLEX DECAY & EUSTACHIAN TUBE FUNCTIONK950637MAICO IN-THE-EAR MODEL RD-312 CICK946253MAICO IN-THE-EAR MODEL RD 201K931322KS 5 - CLINICAL AUDIOMETER

View all 58 devices →

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.

↑