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FDA 510(k)

PHILIPS S1694, S1695

K-Number: K971804 · 1997-06-06

ApplicantPhilips Hearing Instruments Co.
Decision Date1997-06-06
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHILIPS S1694, S1695 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Hearing Instruments Co.. It received FDA 510(k) clearance on 1997-06-06 under 510(k) number K971804. 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 PHILIPS S1694, S1695?

PHILIPS S1694, S1695 is a medical device that received FDA 510(k) clearance on 1997-06-06. The listed applicant is Philips Hearing Instruments Co.. The 510(k) number is K971804.

When did PHILIPS S1694, S1695 receive FDA 510(k) clearance?

PHILIPS S1694, S1695 received FDA 510(k) clearance on 1997-06-06, under 510(k) number K971804.

Who is the listed applicant for PHILIPS S1694, S1695?

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

What is the FDA product code for PHILIPS S1694, S1695?

The FDA product code for PHILIPS S1694, S1695 is ESD.

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Other records listing Philips Hearing Instruments Co. 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.

K972818D72 DIGITALK965088M11 SERIES: M11, M11MK961770PHILIPS 71 SERIESK952658HEARING AIDK944404MO4 SERIESK943670MO6 SERIES

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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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