SA-21 DENTAL UNIT
K-Number: K823180 · 1982-11-22
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Device Summary
Frequently Asked Questions
What is the SA-21 DENTAL UNIT?
SA-21 DENTAL UNIT is a medical device that received FDA 510(k) clearance on 1982-11-22. The listed applicant is Ritter Co.. The 510(k) number is K823180.
When did SA-21 DENTAL UNIT receive FDA 510(k) clearance?
SA-21 DENTAL UNIT received FDA 510(k) clearance on 1982-11-22, under 510(k) number K823180.
Who is the listed applicant for SA-21 DENTAL UNIT?
The FDA 510(k) record lists Ritter Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SA-21 DENTAL UNIT?
The FDA product code for SA-21 DENTAL UNIT is EIA.
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 Ritter Co. 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: EIA)
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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