FD 300 DENTAL STOOL
K-Number: K893944 · 1989-08-15
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Device Summary
Frequently Asked Questions
What is the FD 300 DENTAL STOOL?
FD 300 DENTAL STOOL 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 K893944.
When did FD 300 DENTAL STOOL receive FDA 510(k) clearance?
FD 300 DENTAL STOOL received FDA 510(k) clearance on 1989-08-15, under 510(k) number K893944.
Who is the listed applicant for FD 300 DENTAL STOOL?
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 FD 300 DENTAL STOOL?
The FDA product code for FD 300 DENTAL STOOL 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.
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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