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FDA 510(k)

THE SILENCER

K-Number: K954530 · 1995-10-30

ApplicantSilent Knights Ventures, Inc.
Decision Date1995-10-30
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE SILENCER is the device name listed in this FDA 510(k) record. The listed applicant is Silent Knights Ventures, Inc.. It received FDA 510(k) clearance on 1995-10-30 under 510(k) number K954530. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SILENCER?

THE SILENCER is a medical device that received FDA 510(k) clearance on 1995-10-30. The listed applicant is Silent Knights Ventures, Inc.. The 510(k) number is K954530.

When did THE SILENCER receive FDA 510(k) clearance?

THE SILENCER received FDA 510(k) clearance on 1995-10-30, under 510(k) number K954530.

Who is the listed applicant for THE SILENCER?

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

What is the FDA product code for THE SILENCER?

The FDA product code for THE SILENCER is LRK.

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Related Devices (Code: LRK)

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.

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

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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