DIAMOND STONES
K-Number: K760987 · 1976-11-15
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Device Summary
Frequently Asked Questions
What is the DIAMOND STONES?
DIAMOND STONES is a medical device that received FDA 510(k) clearance on 1976-11-15. The listed applicant is Adp Intl., Inc.. The 510(k) number is K760987.
When did DIAMOND STONES receive FDA 510(k) clearance?
DIAMOND STONES received FDA 510(k) clearance on 1976-11-15, under 510(k) number K760987.
Who is the listed applicant for DIAMOND STONES?
The FDA 510(k) record lists Adp Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAMOND STONES?
The FDA product code for DIAMOND STONES is DZP.
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 Adp Intl., 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: DZP)
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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