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FDA 510(k)

ELGILOY

K-Number: K883074 · 1988-08-09

ApplicantDale T. Dupuis
Decision Date1988-08-09
Product CodeEBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELGILOY is the device name listed in this FDA 510(k) record. The listed applicant is Dale T. Dupuis. It received FDA 510(k) clearance on 1988-08-09 under 510(k) number K883074. The device is classified under product code EBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELGILOY?

ELGILOY is a medical device that received FDA 510(k) clearance on 1988-08-09. The listed applicant is Dale T. Dupuis. The 510(k) number is K883074.

When did ELGILOY receive FDA 510(k) clearance?

ELGILOY received FDA 510(k) clearance on 1988-08-09, under 510(k) number K883074.

Who is the listed applicant for ELGILOY?

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

What is the FDA product code for ELGILOY?

The FDA product code for ELGILOY is EBL.

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.

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Other records listing Dale T. Dupuis 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.

K883388DENTREK BRIDGE BARSK882400AMORPHUS SILK BY DENTRAX

Related Devices (Code: EBL)

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.

K002693CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)Cbs Intl. B.V.K952868DENTAURUM JACKET CROWN & ROOT POSTSDentauraum, Inc.K924376ROOT CANAL POSTThe Thera GroupK895283PROSTHETIC RESTORATION DEVICESwiss Precision Mfg. Corp.K895758PLASTIC TOOTH REINFORCEMENT KITNanzee Dental ProductsK863831VIVADENT FILPINVivadent (Usa), 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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