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FDA 510(k)

ESKA JONAS SILICON-SILVER PENILE

K-Number: K834504 · 1984-02-04

ApplicantDacomed Corp.
Decision Date1984-02-04
Product CodeFAE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ESKA JONAS SILICON-SILVER PENILE is the device name listed in this FDA 510(k) record. The listed applicant is Dacomed Corp.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K834504. The device is classified under product code FAE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESKA JONAS SILICON-SILVER PENILE?

ESKA JONAS SILICON-SILVER PENILE is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Dacomed Corp.. The 510(k) number is K834504.

When did ESKA JONAS SILICON-SILVER PENILE receive FDA 510(k) clearance?

ESKA JONAS SILICON-SILVER PENILE received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834504.

Who is the listed applicant for ESKA JONAS SILICON-SILVER PENILE?

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 ESKA JONAS SILICON-SILVER PENILE?

The FDA product code for ESKA JONAS SILICON-SILVER PENILE is FAE.

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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: FAE)

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.

K183619Tactra Penile Prosthesis, 9.5 mm Device, Tactra Penile Prosthesis, 11 mm Device, Tactra Penile Prosthesis, 13 mm DeviceBoston Scientific CorporationK181673Rigi10 Malleable Penile ProsthesisRigicon, Inc.K090663AMS SPECTRA CONCEALABLE PENILE PROSTHESISAmerican Medical Systems, Inc.K082006AMS SPECTRA CONCEALABLE PENILE PROSTHESISAmerican Medical Systems, Inc.K040959MENTOR GENESIS PENILE PROSTHESISMentor Corp.K963328AMS AMBICOR PENILE PROSTHESISAmerican Medical Systems, 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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