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FDA 510(k)

ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS

K-Number: K983285 · 1998-11-04

Decision Date1998-11-04
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Engle Dental Systems. It received FDA 510(k) clearance on 1998-11-04 under 510(k) number K983285. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS?

ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS is a medical device that received FDA 510(k) clearance on 1998-11-04. The listed applicant is Engle Dental Systems. The 510(k) number is K983285.

When did ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS receive FDA 510(k) clearance?

ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS received FDA 510(k) clearance on 1998-11-04, under 510(k) number K983285.

Who is the listed applicant for ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS?

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

What is the FDA product code for ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS?

The FDA product code for ENGLE DENTAL FAMILY OF DELIVERY SYSTEMS is EIA.

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.

Related Devices (Code: EIA)

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.

Official Source

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