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FDA 510(k)

MEGA-SIL A-B

K-Number: K950912 · 1995-03-21

ApplicantMicrosonic, Inc.
Decision Date1995-03-21
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MEGA-SIL A-B is the device name listed in this FDA 510(k) record. The listed applicant is Microsonic, Inc.. It received FDA 510(k) clearance on 1995-03-21 under 510(k) number K950912. 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 MEGA-SIL A-B?

MEGA-SIL A-B is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Microsonic, Inc.. The 510(k) number is K950912.

When did MEGA-SIL A-B receive FDA 510(k) clearance?

MEGA-SIL A-B received FDA 510(k) clearance on 1995-03-21, under 510(k) number K950912.

Who is the listed applicant for MEGA-SIL A-B?

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

What is the FDA product code for MEGA-SIL A-B?

The FDA product code for MEGA-SIL A-B is ESD.

Other records listing Microsonic, 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.

K945255MICROSIL

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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