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)

PHILIPS M60 SERIES

K-Number: K920142 · 1992-01-23

ApplicantPhilips Int'L B.V.
Decision Date1992-01-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHILIPS M60 SERIES 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 1992-01-23 under 510(k) number K920142. 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 M60 SERIES?

PHILIPS M60 SERIES is a medical device that received FDA 510(k) clearance on 1992-01-23. The listed applicant is Philips Int'L B.V.. The 510(k) number is K920142.

When did PHILIPS M60 SERIES receive FDA 510(k) clearance?

PHILIPS M60 SERIES received FDA 510(k) clearance on 1992-01-23, under 510(k) number K920142.

Who is the listed applicant for PHILIPS M60 SERIES?

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 M60 SERIES?

The FDA product code for PHILIPS M60 SERIES 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 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.

K920134PHILIPS 41 SERIES RAINBOWK852348PHILIPS 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

View all 11 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.

↑