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FDA 510(k)

PORTABLE II DENTAL DELIVERY SYSTEM

K-Number: K883775 · 1988-10-14

ApplicantDntl Corp.
Decision Date1988-10-14
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORTABLE II DENTAL DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dntl Corp.. It received FDA 510(k) clearance on 1988-10-14 under 510(k) number K883775. 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 PORTABLE II DENTAL DELIVERY SYSTEM?

PORTABLE II DENTAL DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1988-10-14. The listed applicant is Dntl Corp.. The 510(k) number is K883775.

When did PORTABLE II DENTAL DELIVERY SYSTEM receive FDA 510(k) clearance?

PORTABLE II DENTAL DELIVERY SYSTEM received FDA 510(k) clearance on 1988-10-14, under 510(k) number K883775.

Who is the listed applicant for PORTABLE II DENTAL DELIVERY SYSTEM?

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

What is the FDA product code for PORTABLE II DENTAL DELIVERY SYSTEM?

The FDA product code for PORTABLE II DENTAL DELIVERY SYSTEM 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.

Other records listing Dntl Corp. 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.

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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