BEACH ANESTHETIC SYRINGE CARTR. TYPE
K-Number: K821782 · 1982-07-20
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Device Summary
Frequently Asked Questions
What is the BEACH ANESTHETIC SYRINGE CARTR. TYPE?
BEACH ANESTHETIC SYRINGE CARTR. TYPE is a medical device that received FDA 510(k) clearance on 1982-07-20. The listed applicant is Pacific Dental Corp.. The 510(k) number is K821782.
When did BEACH ANESTHETIC SYRINGE CARTR. TYPE receive FDA 510(k) clearance?
BEACH ANESTHETIC SYRINGE CARTR. TYPE received FDA 510(k) clearance on 1982-07-20, under 510(k) number K821782.
Who is the listed applicant for BEACH ANESTHETIC SYRINGE CARTR. TYPE?
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 ANESTHETIC SYRINGE CARTR. TYPE?
The FDA product code for BEACH ANESTHETIC SYRINGE CARTR. TYPE is EJI.
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: EJI)
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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