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FDA 510(k)

NAPA

K-Number: K902790 · 1990-09-19

ApplicantG-Ortho Lab
Decision Date1990-09-19
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NAPA is the device name listed in this FDA 510(k) record. The listed applicant is G-Ortho Lab. It received FDA 510(k) clearance on 1990-09-19 under 510(k) number K902790. 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 NAPA?

NAPA is a medical device that received FDA 510(k) clearance on 1990-09-19. The listed applicant is G-Ortho Lab. The 510(k) number is K902790.

When did NAPA receive FDA 510(k) clearance?

NAPA received FDA 510(k) clearance on 1990-09-19, under 510(k) number K902790.

Who is the listed applicant for NAPA?

The FDA 510(k) record lists G-Ortho Lab as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAPA?

The FDA product code for NAPA 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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