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FDA 510(k)

OSAP

K-Number: K960673 · 1996-05-09

ApplicantSnorefree, Inc.
Decision Date1996-05-09
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OSAP is the device name listed in this FDA 510(k) record. The listed applicant is Snorefree, Inc.. It received FDA 510(k) clearance on 1996-05-09 under 510(k) number K960673. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSAP?

OSAP is a medical device that received FDA 510(k) clearance on 1996-05-09. The listed applicant is Snorefree, Inc.. The 510(k) number is K960673.

When did OSAP receive FDA 510(k) clearance?

OSAP received FDA 510(k) clearance on 1996-05-09, under 510(k) number K960673.

Who is the listed applicant for OSAP?

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

What is the FDA product code for OSAP?

The FDA product code for OSAP is LQZ.

Related Devices (Code: LQZ)

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.

K233754AIO BreatheAiomega, LLCK230532RADx Intraoral Appliance for Snoring and Sleep ApneaAchaemenid, LLCK203712The SlideBiotex, Inc.K191320Slow Wave DS8Slow Wave, Inc.K192581The NightBlocks ApplianceAdvanced Facialdontics, LLCK162816SML-OSA2 AppliancesSelane Products, Inc.

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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