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FDA 510(k)

TAP ANTI-SNORING DEVICE

K-Number: K962516 · 1996-09-10

ApplicantNellcor Puritan Bennett, Inc.
Decision Date1996-09-10
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TAP ANTI-SNORING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Nellcor Puritan Bennett, Inc.. It received FDA 510(k) clearance on 1996-09-10 under 510(k) number K962516. 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 TAP ANTI-SNORING DEVICE?

TAP ANTI-SNORING DEVICE is a medical device that received FDA 510(k) clearance on 1996-09-10. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K962516.

When did TAP ANTI-SNORING DEVICE receive FDA 510(k) clearance?

TAP ANTI-SNORING DEVICE received FDA 510(k) clearance on 1996-09-10, under 510(k) number K962516.

Who is the listed applicant for TAP ANTI-SNORING DEVICE?

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

What is the FDA product code for TAP ANTI-SNORING DEVICE?

The FDA product code for TAP ANTI-SNORING DEVICE is LRK.

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Other records listing Nellcor Puritan Bennett, 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.

K070408DURAMAX REUSABLE OXIMETRY SENSORK060576NELLCOR OXIMAX N-600X PULSE OXIMETERK051271OXIMAX NEOMAX ADHESIVE FOREHEAD REFLECTANCE OXIMETRY SENSORK052186NELLCOR OXIMAX PULSE OXIMETRY SENSONS (MAX-A, MAX-AL, MAX-N, MAX-I, MAX-PK051352OXIMAX NPB-40 HANDHELD PULSE OXIMETERK050072GOODKNIGHT 425ST

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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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