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FDA 510(k)

PENILE ERECTION MONITOR

K-Number: K810944 · 1981-04-23

ApplicantMedical Monitoring Systems, Inc.
Decision Date1981-04-23
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

PENILE ERECTION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Monitoring Systems, Inc.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810944. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENILE ERECTION MONITOR?

PENILE ERECTION MONITOR is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Medical Monitoring Systems, Inc.. The 510(k) number is K810944.

When did PENILE ERECTION MONITOR receive FDA 510(k) clearance?

PENILE ERECTION MONITOR received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810944.

Who is the listed applicant for PENILE ERECTION MONITOR?

The FDA 510(k) record lists Medical Monitoring Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PENILE ERECTION MONITOR?

The FDA product code for PENILE ERECTION MONITOR 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Monitoring Systems, 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.

K841879LFT - 212

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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