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FDA 510(k)

SNORE TEC

K-Number: K963063 · 1997-04-14

ApplicantMarketing Technologies, Inc.
Decision Date1997-04-14
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNORE TEC is the device name listed in this FDA 510(k) record. The listed applicant is Marketing Technologies, Inc.. It received FDA 510(k) clearance on 1997-04-14 under 510(k) number K963063. 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 SNORE TEC?

SNORE TEC is a medical device that received FDA 510(k) clearance on 1997-04-14. The listed applicant is Marketing Technologies, Inc.. The 510(k) number is K963063.

When did SNORE TEC receive FDA 510(k) clearance?

SNORE TEC received FDA 510(k) clearance on 1997-04-14, under 510(k) number K963063.

Who is the listed applicant for SNORE TEC?

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

What is the FDA product code for SNORE TEC?

The FDA product code for SNORE TEC 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.

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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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