LYNX DPA DISPOSABLE PROPHY ANGLE
K-Number: K960541 · 1996-03-28
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Device Summary
Frequently Asked Questions
What is the LYNX DPA DISPOSABLE PROPHY ANGLE?
LYNX DPA DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Mti Precision Products. The 510(k) number is K960541.
When did LYNX DPA DISPOSABLE PROPHY ANGLE receive FDA 510(k) clearance?
LYNX DPA DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 1996-03-28, under 510(k) number K960541.
Who is the listed applicant for LYNX DPA DISPOSABLE PROPHY ANGLE?
The FDA 510(k) record lists Mti Precision Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LYNX DPA DISPOSABLE PROPHY ANGLE?
The FDA product code for LYNX DPA DISPOSABLE PROPHY ANGLE is EFB.
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 Mti Precision Products 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: EFB)
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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