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)

ACQUASEAL BENZ

K-Number: K070289 · 2007-05-04

ApplicantAcquamed Technologies, Inc.
Decision Date2007-05-04
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACQUASEAL BENZ is the device name listed in this FDA 510(k) record. The listed applicant is Acquamed Technologies, Inc.. It received FDA 510(k) clearance on 2007-05-04 under 510(k) number K070289. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACQUASEAL BENZ?

ACQUASEAL BENZ is a medical device that received FDA 510(k) clearance on 2007-05-04. The listed applicant is Acquamed Technologies, Inc.. The 510(k) number is K070289.

When did ACQUASEAL BENZ receive FDA 510(k) clearance?

ACQUASEAL BENZ received FDA 510(k) clearance on 2007-05-04, under 510(k) number K070289.

Who is the listed applicant for ACQUASEAL BENZ?

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

What is the FDA product code for ACQUASEAL BENZ?

The FDA product code for ACQUASEAL BENZ is LBH.

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: LBH)

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.

K262243Profisil FreeKettenbach GmbH & Co. KGK253052Fluoride Varnish (Type A,Type C)Nagy Oral Technology Qinhuangdao Co., Ltd.K252073VOCO Profluorid Varnish + BioMinVoco GmbHK261404UltraEZUltradent Products, Inc.K260830APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)Sangi Co., Ltd.K250714FluoroDose VarnishCentrix, 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.

↑