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FDA 510(k)

PHILIPS 41 SERIES RAINBOW

K-Number: K920134 · 1992-01-24

ApplicantPhilips Int'L B.V.
Decision Date1992-01-24
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHILIPS 41 SERIES RAINBOW is the device name listed in this FDA 510(k) record. The listed applicant is Philips Int'L B.V.. It received FDA 510(k) clearance on 1992-01-24 under 510(k) number K920134. 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 41 SERIES RAINBOW?

PHILIPS 41 SERIES RAINBOW is a medical device that received FDA 510(k) clearance on 1992-01-24. The listed applicant is Philips Int'L B.V.. The 510(k) number is K920134.

When did PHILIPS 41 SERIES RAINBOW receive FDA 510(k) clearance?

PHILIPS 41 SERIES RAINBOW received FDA 510(k) clearance on 1992-01-24, under 510(k) number K920134.

Who is the listed applicant for PHILIPS 41 SERIES RAINBOW?

The FDA 510(k) record lists Philips Int'L B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS 41 SERIES RAINBOW?

The FDA product code for PHILIPS 41 SERIES RAINBOW is ESD.

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Other records listing Philips Int'L B.V. 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.

K920142PHILIPS M60 SERIESK852348PHILIPS SOLARIUM HP 3134K851536PHILIPS UV-A SOLARIUM TYPE HP 3141K851534PHILIPS UV-A SOLARIUM TYPE HP 3150K851533PHILIPS UV-A SDARIUM TYPE HP 3148(CFR 21 SUNLAMPK851535PHILIPS UV-A SOLARIUM TYPE HP 3140

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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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