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FDA 510(k)

OXI-SNAP

K-Number: K971184 · 1997-10-01

ApplicantSnap Laboratories, LLC
Decision Date1997-10-01
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXI-SNAP is the device name listed in this FDA 510(k) record. The listed applicant is Snap Laboratories, LLC. It received FDA 510(k) clearance on 1997-10-01 under 510(k) number K971184. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXI-SNAP?

OXI-SNAP is a medical device that received FDA 510(k) clearance on 1997-10-01. The listed applicant is Snap Laboratories, LLC. The 510(k) number is K971184.

When did OXI-SNAP receive FDA 510(k) clearance?

OXI-SNAP received FDA 510(k) clearance on 1997-10-01, under 510(k) number K971184.

Who is the listed applicant for OXI-SNAP?

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

What is the FDA product code for OXI-SNAP?

The FDA product code for OXI-SNAP is MNR.

Other records listing Snap Laboratories, LLC 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.

K080321SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEMK002095SNAP MODEL 6K992322SNAP MODEL 5K984169DIGI-SNAPK944524SNAP TESTING DEVICE

Related Devices (Code: MNR)

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.

K260949Disposable Belts for Polysomnography (CNSAC)CNSAC Medshop GmbHK254042WatchPAT SWItamar Medical , Ltd.K260050WRAP SystemHuneo, LLCK253148RX-1 SleepVivaquant, Inc. Dba Rhythm ExpressK252628CASSIEWesper, Inc.K252497SANSA HSATHuxley Medical

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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