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FDA 510(k)

DACOMED RIGISCAN SYSTEM

K-Number: K841202 · 1984-07-06

ApplicantDacomed Corp.
Decision Date1984-07-06
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

DACOMED RIGISCAN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dacomed Corp.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K841202. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DACOMED RIGISCAN SYSTEM?

DACOMED RIGISCAN SYSTEM is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Dacomed Corp.. The 510(k) number is K841202.

When did DACOMED RIGISCAN SYSTEM receive FDA 510(k) clearance?

DACOMED RIGISCAN SYSTEM received FDA 510(k) clearance on 1984-07-06, under 510(k) number K841202.

Who is the listed applicant for DACOMED RIGISCAN SYSTEM?

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

What is the FDA product code for DACOMED RIGISCAN SYSTEM?

The FDA product code for DACOMED RIGISCAN SYSTEM is LIL.

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Other records listing Dacomed Corp. 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.

K953640DUNA II PENILE PROSTHESISK941781RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEMK920409DACOMED BATTERY OPERATED VACUUM ERECTION DEVICEK920420DURA II PENILE PROSTHESISK912344MODIFIED DURAPHASE(TM) IMPLANTED PENILE PROSTHESISK900774DACOMED NEGATIVE PRESSURE ERECTION DEVICE

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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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