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 DELIVERY SYSTEM

K-Number: K896532 · 1990-02-12

ApplicantDentech Corp.
Decision Date1990-02-12
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dentech Corp.. It received FDA 510(k) clearance on 1990-02-12 under 510(k) number K896532. 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 DENTAL DELIVERY SYSTEM?

DENTAL DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1990-02-12. The listed applicant is Dentech Corp.. The 510(k) number is K896532.

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

DENTAL DELIVERY SYSTEM received FDA 510(k) clearance on 1990-02-12, under 510(k) number K896532.

Who is the listed applicant for DENTAL DELIVERY SYSTEM?

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

What is the FDA product code for DENTAL DELIVERY SYSTEM?

The FDA product code for 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 Dentech 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

View on FDA Database →

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

↑