ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL
K-Number: K820574 · 1982-03-23
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Device Summary
Frequently Asked Questions
What is the ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL?
ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL is a medical device that received FDA 510(k) clearance on 1982-03-23. The listed applicant is David Simmonds Co., Inc.. The 510(k) number is K820574.
When did ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL receive FDA 510(k) clearance?
ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL received FDA 510(k) clearance on 1982-03-23, under 510(k) number K820574.
Who is the listed applicant for ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL?
The FDA 510(k) record lists David Simmonds Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL?
The FDA product code for ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL is BWN.
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 David Simmonds Co., Inc. 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: BWN)
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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