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FDA 510(k)

FD3500 (DENTAL CHAIR)

K-Number: K893889 · 1989-08-15

Decision Date1989-08-15
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FD3500 (DENTAL CHAIR) is the device name listed in this FDA 510(k) record. The listed applicant is Oriola OY Finndent. It received FDA 510(k) clearance on 1989-08-15 under 510(k) number K893889. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FD3500 (DENTAL CHAIR)?

FD3500 (DENTAL CHAIR) is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Oriola OY Finndent. The 510(k) number is K893889.

When did FD3500 (DENTAL CHAIR) receive FDA 510(k) clearance?

FD3500 (DENTAL CHAIR) received FDA 510(k) clearance on 1989-08-15, under 510(k) number K893889.

Who is the listed applicant for FD3500 (DENTAL CHAIR)?

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

What is the FDA product code for FD3500 (DENTAL CHAIR)?

The FDA product code for FD3500 (DENTAL CHAIR) is KLC.

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 Oriola OY Finndent 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: KLC)

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.

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