RT2 RIGIDITY AND TUMESCENCE TEST
K-Number: K925931 · 1992-12-21
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Device Summary
Frequently Asked Questions
What is the RT2 RIGIDITY AND TUMESCENCE TEST?
RT2 RIGIDITY AND TUMESCENCE TEST is a medical device that received FDA 510(k) clearance on 1992-12-21. The listed applicant is Compass Medical Technologies, Inc.. The 510(k) number is K925931.
When did RT2 RIGIDITY AND TUMESCENCE TEST receive FDA 510(k) clearance?
RT2 RIGIDITY AND TUMESCENCE TEST received FDA 510(k) clearance on 1992-12-21, under 510(k) number K925931.
Who is the listed applicant for RT2 RIGIDITY AND TUMESCENCE TEST?
The FDA 510(k) record lists Compass Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RT2 RIGIDITY AND TUMESCENCE TEST?
The FDA product code for RT2 RIGIDITY AND TUMESCENCE TEST is LIL.
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.
Related Devices (Code: LIL)
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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