Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TGO SPRAY

K-Number: K051812 · 2005-10-21

ApplicantLaboratoires Carilene S.A.S.
Decision Date2005-10-21
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

TGO SPRAY is the device name listed in this FDA 510(k) record. The listed applicant is Laboratoires Carilene S.A.S.. It received FDA 510(k) clearance on 2005-10-21 under 510(k) number K051812. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TGO SPRAY?

TGO SPRAY is a medical device that received FDA 510(k) clearance on 2005-10-21. The listed applicant is Laboratoires Carilene S.A.S.. The 510(k) number is K051812.

When did TGO SPRAY receive FDA 510(k) clearance?

TGO SPRAY received FDA 510(k) clearance on 2005-10-21, under 510(k) number K051812.

Who is the listed applicant for TGO SPRAY?

The FDA 510(k) record lists Laboratoires Carilene S.A.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TGO SPRAY?

The FDA product code for TGO SPRAY is LFD.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: LFD)

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.

K253778Allday Moisturizing RinseElevate Oral CareK250390CloSYS® 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) LimitedK231205GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral SprayGurunanda, LLCK202689Dentilube SprayOxy2plus, LLC

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.

↑