BEACH MOUTH MIRROR
K-Number: K821777 · 1982-07-06
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Device Summary
Frequently Asked Questions
What is the BEACH MOUTH MIRROR?
BEACH MOUTH MIRROR is a medical device that received FDA 510(k) clearance on 1982-07-06. The listed applicant is Pacific Dental Corp.. The 510(k) number is K821777.
When did BEACH MOUTH MIRROR receive FDA 510(k) clearance?
BEACH MOUTH MIRROR received FDA 510(k) clearance on 1982-07-06, under 510(k) number K821777.
Who is the listed applicant for BEACH MOUTH MIRROR?
The FDA 510(k) record lists Pacific Dental Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEACH MOUTH MIRROR?
The FDA product code for BEACH MOUTH MIRROR is EAX.
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 Pacific Dental Corp. 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: EAX)
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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