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)

S-FILE, S-FINDER, S-ENGINE FILE

K-Number: K892894 · 1989-05-24

Decision Date1989-05-24
Product CodeEKS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

S-FILE, S-FINDER, S-ENGINE FILE is the device name listed in this FDA 510(k) record. The listed applicant is Svenska Dental Instruments AB. It received FDA 510(k) clearance on 1989-05-24 under 510(k) number K892894. The device is classified under product code EKS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S-FILE, S-FINDER, S-ENGINE FILE?

S-FILE, S-FINDER, S-ENGINE FILE is a medical device that received FDA 510(k) clearance on 1989-05-24. The listed applicant is Svenska Dental Instruments AB. The 510(k) number is K892894.

When did S-FILE, S-FINDER, S-ENGINE FILE receive FDA 510(k) clearance?

S-FILE, S-FINDER, S-ENGINE FILE received FDA 510(k) clearance on 1989-05-24, under 510(k) number K892894.

Who is the listed applicant for S-FILE, S-FINDER, S-ENGINE FILE?

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

What is the FDA product code for S-FILE, S-FINDER, S-ENGINE FILE?

The FDA product code for S-FILE, S-FINDER, S-ENGINE FILE is EKS.

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 Svenska Dental Instruments AB 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: EKS)

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.

↑