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FDA 510(k)

SNAP MODEL 6

K-Number: K002095 · 2001-03-02

ApplicantSnap Laboratories, LLC
Decision Date2001-03-02
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SNAP MODEL 6 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 2001-03-02 under 510(k) number K002095. 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 MODEL 6?

SNAP MODEL 6 is a medical device that received FDA 510(k) clearance on 2001-03-02. The listed applicant is Snap Laboratories, LLC. The 510(k) number is K002095.

When did SNAP MODEL 6 receive FDA 510(k) clearance?

SNAP MODEL 6 received FDA 510(k) clearance on 2001-03-02, under 510(k) number K002095.

Who is the listed applicant for SNAP MODEL 6?

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 MODEL 6?

The FDA product code for SNAP MODEL 6 is MNR.

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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 SYSTEMK992322SNAP MODEL 5K984169DIGI-SNAPK971184OXI-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.

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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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