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 DIGITAL PANORAMIC/3D IMAGING SYSTEM

K-Number: K070658 · 2007-04-05

Decision Date2007-04-05
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is E-Woo Technology. It received FDA 510(k) clearance on 2007-04-05 under 510(k) number K070658. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM?

DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2007-04-05. The listed applicant is E-Woo Technology. The 510(k) number is K070658.

When did DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM receive FDA 510(k) clearance?

DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM received FDA 510(k) clearance on 2007-04-05, under 510(k) number K070658.

Who is the listed applicant for DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM?

The FDA 510(k) record lists E-Woo Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM?

The FDA product code for DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEM is JAK.

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 E-Woo Technology 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.

View all 7 devices →

Related Devices (Code: JAK)

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.

↑