DISPOSABLE PROPHYLAXIS ANGLE
K-Number: K951016 · 1995-05-02
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE PROPHYLAXIS ANGLE?
DISPOSABLE PROPHYLAXIS ANGLE is a medical device that received FDA 510(k) clearance on 1995-05-02. The listed applicant is Preventive Technologies, Inc.. The 510(k) number is K951016.
When did DISPOSABLE PROPHYLAXIS ANGLE receive FDA 510(k) clearance?
DISPOSABLE PROPHYLAXIS ANGLE received FDA 510(k) clearance on 1995-05-02, under 510(k) number K951016.
Who is the listed applicant for DISPOSABLE PROPHYLAXIS ANGLE?
The FDA 510(k) record lists Preventive Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE PROPHYLAXIS ANGLE?
The FDA product code for DISPOSABLE PROPHYLAXIS ANGLE is EHK.
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 Preventive Technologies, 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: EHK)
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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