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FDA 510(k)

PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)

K-Number: K062042 · 2006-09-06

ApplicantPlethora Solutions
Decision Date2006-09-06
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM) is the device name listed in this FDA 510(k) record. The listed applicant is Plethora Solutions. It received FDA 510(k) clearance on 2006-09-06 under 510(k) number K062042. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)?

PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM) is a medical device that received FDA 510(k) clearance on 2006-09-06. The listed applicant is Plethora Solutions. The 510(k) number is K062042.

When did PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM) receive FDA 510(k) clearance?

PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM) received FDA 510(k) clearance on 2006-09-06, under 510(k) number K062042.

Who is the listed applicant for PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)?

The FDA 510(k) record lists Plethora Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)?

The FDA product code for PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM) 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.

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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 21K052929PREFTEST PROFESSIONAL SUITELimestone Technologies, Inc.K033126MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEMBehavioral Technology, Inc.K000194DIGITAL INFLECTION RIGIDOMETER (DIR)Uroan Xxi ElectromedicinaK991479VISER PENILE TUMESCENCE MONITORLaborie Medical Tech Corp.K980627NEVA SYSTEMUrometrics, Inc.

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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