CAT-400UL PENILE PLETHYSMOGRAPH
K-Number: K940128 · 1995-01-10
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Device Summary
Frequently Asked Questions
What is the CAT-400UL PENILE PLETHYSMOGRAPH?
CAT-400UL PENILE PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1995-01-10. The listed applicant is Farrall Instruments, Inc.. The 510(k) number is K940128.
When did CAT-400UL PENILE PLETHYSMOGRAPH receive FDA 510(k) clearance?
CAT-400UL PENILE PLETHYSMOGRAPH received FDA 510(k) clearance on 1995-01-10, under 510(k) number K940128.
Who is the listed applicant for CAT-400UL PENILE PLETHYSMOGRAPH?
The FDA 510(k) record lists Farrall Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAT-400UL PENILE PLETHYSMOGRAPH?
The FDA product code for CAT-400UL PENILE PLETHYSMOGRAPH 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.
Other records listing Farrall Instruments, 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: 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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