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FDA 510(k)

CAT-600 PENILE PLETHYSMOGRAPH

K-Number: K936115 · 1995-01-10

ApplicantFarrall Instruments, Inc.
Decision Date1995-01-10
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

CAT-600 PENILE PLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Farrall Instruments, Inc.. It received FDA 510(k) clearance on 1995-01-10 under 510(k) number K936115. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAT-600 PENILE PLETHYSMOGRAPH?

CAT-600 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 K936115.

When did CAT-600 PENILE PLETHYSMOGRAPH receive FDA 510(k) clearance?

CAT-600 PENILE PLETHYSMOGRAPH received FDA 510(k) clearance on 1995-01-10, under 510(k) number K936115.

Who is the listed applicant for CAT-600 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-600 PENILE PLETHYSMOGRAPH?

The FDA product code for CAT-600 PENILE PLETHYSMOGRAPH is LIL.

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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.

K940128CAT-400UL PENILE PLETHYSMOGRAPHK821723BI-4520 DUAL IMPEDOMETERK821664PP-100, PERSONAL PERINEOMETERK792305A SLEEP ASSESSMENT DEVICEK781634VISUALAXK760166STIMULATOR, SONIC CONTROL (AS-1)

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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.

K061676RIGIDOMETER, MODEL DIR-4UUroan 21K062042PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)Plethora SolutionsK052929PREFTEST PROFESSIONAL SUITELimestone Technologies, Inc.K033126MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEMBehavioral Technology, Inc.K000194DIGITAL INFLECTION RIGIDOMETER (DIR)Uroan Xxi ElectromedicinaK991479VISER PENILE TUMESCENCE MONITORLaborie Medical Tech Corp.

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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