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FDA 510(k)

SNAP TESTING DEVICE

K-Number: K944524 · 1995-10-26

ApplicantSnap Laboratories, LLC
Decision Date1995-10-26
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SNAP TESTING DEVICE 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 1995-10-26 under 510(k) number K944524. 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 SNAP TESTING DEVICE?

SNAP TESTING DEVICE is a medical device that received FDA 510(k) clearance on 1995-10-26. The listed applicant is Snap Laboratories, LLC. The 510(k) number is K944524.

When did SNAP TESTING DEVICE receive FDA 510(k) clearance?

SNAP TESTING DEVICE received FDA 510(k) clearance on 1995-10-26, under 510(k) number K944524.

Who is the listed applicant for SNAP TESTING DEVICE?

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 SNAP TESTING DEVICE?

The FDA product code for SNAP TESTING DEVICE is MNR.

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 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-SNAPK971184OXI-SNAP

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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