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FDA 510(k)

VIP

K-Number: K950080 · 1995-02-08

ApplicantBell Hearing Instruments, Inc.
Decision Date1995-02-08
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VIP is the device name listed in this FDA 510(k) record. The listed applicant is Bell Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1995-02-08 under 510(k) number K950080. 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 VIP?

VIP is a medical device that received FDA 510(k) clearance on 1995-02-08. The listed applicant is Bell Hearing Instruments, Inc.. The 510(k) number is K950080.

When did VIP receive FDA 510(k) clearance?

VIP received FDA 510(k) clearance on 1995-02-08, under 510(k) number K950080.

Who is the listed applicant for VIP?

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

What is the FDA product code for VIP?

The FDA product code for VIP is ESD.

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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