BEACH FORCEP NO. 150 AND NO. 151
K-Number: K821781 · 1982-07-02
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Device Summary
Frequently Asked Questions
What is the BEACH FORCEP NO. 150 AND NO. 151?
BEACH FORCEP NO. 150 AND NO. 151 is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Pacific Dental Corp.. The 510(k) number is K821781.
When did BEACH FORCEP NO. 150 AND NO. 151 receive FDA 510(k) clearance?
BEACH FORCEP NO. 150 AND NO. 151 received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821781.
Who is the listed applicant for BEACH FORCEP NO. 150 AND NO. 151?
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 FORCEP NO. 150 AND NO. 151?
The FDA product code for BEACH FORCEP NO. 150 AND NO. 151 is EMG.
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: EMG)
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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