BEACH SURGICAL PLIERS NON-HOOK
K-Number: K821787 · 1982-07-06
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Device Summary
Frequently Asked Questions
What is the BEACH SURGICAL PLIERS NON-HOOK?
BEACH SURGICAL PLIERS NON-HOOK 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 K821787.
When did BEACH SURGICAL PLIERS NON-HOOK receive FDA 510(k) clearance?
BEACH SURGICAL PLIERS NON-HOOK received FDA 510(k) clearance on 1982-07-06, under 510(k) number K821787.
Who is the listed applicant for BEACH SURGICAL PLIERS NON-HOOK?
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 SURGICAL PLIERS NON-HOOK?
The FDA product code for BEACH SURGICAL PLIERS NON-HOOK is EJY.
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: EJY)
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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