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)

DENTAL-QUECKSILBER (DENTAL MERCURY)

K-Number: K902388 · 1990-06-28

ApplicantDegussa AG
Decision Date1990-06-28
Product CodeELY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL-QUECKSILBER (DENTAL MERCURY) is the device name listed in this FDA 510(k) record. The listed applicant is Degussa AG. It received FDA 510(k) clearance on 1990-06-28 under 510(k) number K902388. The device is classified under product code ELY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL-QUECKSILBER (DENTAL MERCURY)?

DENTAL-QUECKSILBER (DENTAL MERCURY) is a medical device that received FDA 510(k) clearance on 1990-06-28. The listed applicant is Degussa AG. The 510(k) number is K902388.

When did DENTAL-QUECKSILBER (DENTAL MERCURY) receive FDA 510(k) clearance?

DENTAL-QUECKSILBER (DENTAL MERCURY) received FDA 510(k) clearance on 1990-06-28, under 510(k) number K902388.

Who is the listed applicant for DENTAL-QUECKSILBER (DENTAL MERCURY)?

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

What is the FDA product code for DENTAL-QUECKSILBER (DENTAL MERCURY)?

The FDA product code for DENTAL-QUECKSILBER (DENTAL MERCURY) is ELY.

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

Other records listing Degussa AG as applicant

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.

K953344DEGUBOND ULTRAK931808DUCERAGOLD, DUCERATINK926347DUCERANIUM UK922790DEGUCAST 40K921772BIOLORK921479DUCERATIN/DUCERAM LFC DENTAL PORCELAIN

View all 33 devices →

Related Devices (Code: ELY)

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.

K093587DENTAL MERCURYDmg USA, Inc.K973548MERCURY DENTALAleaciones Dentales Zeyco, S.A. DE C.V.K913814MODEL #05 ANEROID SPHYGMOMANOMETER KITNational Health-Care Equipment, 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.

↑