FDA 510(k)

Lubricity

Numéro K : K163476 · 2017-05-10

DemandeurYou First Services, Incorporated

Date de décision2017-05-10

Code produitLFD

DécisionSubstantially Equivalent

Résumé du dispositif

Lubricity is the device name listed in this FDA 510(k) record. The listed applicant is You First Services, Incorporated. It received FDA 510(k) clearance on 2017-05-10 under 510(k) number K163476. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Lubricity?

Lubricity is a medical device that received FDA 510(k) clearance on 2017-05-10. The listed applicant is You First Services, Incorporated. The 510(k) number is K163476.

When did Lubricity receive FDA 510(k) clearance?

Lubricity received FDA 510(k) clearance on 2017-05-10, under 510(k) number K163476.

Who is the listed applicant for Lubricity?

The FDA 510(k) record lists You First Services, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lubricity?

The FDA product code for Lubricity is LFD.

Essais cliniques associés

Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Dispositifs connexes (Code : LFD)

K253778Allday Moisturizing RinseElevate Oral Care K250390CloSYS® Dry Mouth Sensitive Mouth RinseRowpar Pharmaceuticals, Inc.K240508Salivea Dry Mouth Moisturizing Gel (Dry Mouth Moisturizing Gel)Laclede, Inc.K234015Caphosol® Artifical Saliva (32 doses sachet box)Eusa Pharma (Uk) Limited K231205GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral SprayGurunanda, LLC K202689Dentilube SprayOxy2plus, LLC

Source officielle

Voir dans la base de données FDA →

Données issues de l'API ouverte de la FDA. Pour les informations les plus récentes et faisant autorité, veuillez toujours vous référer au registre officiel.