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)

STAR TITAN SERIES MOTORS & ATTACHMENTS

K-Number: K960260 · 1996-03-28

Decision Date1996-03-28
Product CodeEFA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STAR TITAN SERIES MOTORS & ATTACHMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Dentalez Group. It received FDA 510(k) clearance on 1996-03-28 under 510(k) number K960260. The device is classified under product code EFA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAR TITAN SERIES MOTORS & ATTACHMENTS?

STAR TITAN SERIES MOTORS & ATTACHMENTS is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Dentalez Group. The 510(k) number is K960260.

When did STAR TITAN SERIES MOTORS & ATTACHMENTS receive FDA 510(k) clearance?

STAR TITAN SERIES MOTORS & ATTACHMENTS received FDA 510(k) clearance on 1996-03-28, under 510(k) number K960260.

Who is the listed applicant for STAR TITAN SERIES MOTORS & ATTACHMENTS?

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

What is the FDA product code for STAR TITAN SERIES MOTORS & ATTACHMENTS?

The FDA product code for STAR TITAN SERIES MOTORS & ATTACHMENTS is EFA.

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 Dentalez Group 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 13 devices →

Related Devices (Code: EFA)

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.

↑