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FDA 510(k)

MENTOR CORPORAL DILATORS

K-Number: K860517 · 1986-03-11

ApplicantMentor Corp.
Decision Date1986-03-11
Product CodeFAE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MENTOR CORPORAL DILATORS is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1986-03-11 under 510(k) number K860517. 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 MENTOR CORPORAL DILATORS?

MENTOR CORPORAL DILATORS is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is Mentor Corp.. The 510(k) number is K860517.

When did MENTOR CORPORAL DILATORS receive FDA 510(k) clearance?

MENTOR CORPORAL DILATORS received FDA 510(k) clearance on 1986-03-11, under 510(k) number K860517.

Who is the listed applicant for MENTOR CORPORAL DILATORS?

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

What is the FDA product code for MENTOR CORPORAL DILATORS?

The FDA product code for MENTOR CORPORAL DILATORS is FAE.

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Other records listing Mentor 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.

K130813MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXPANDERSK053414MENTOR NOVASILK MESHK050008MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETERK042851MENTOR OBTAPE TRANS-OBTURATOR SURGICAL KITK040959MENTOR GENESIS PENILE PROSTHESISK031767MENTOR OBTAPE TRANS-OBTURATOR TAPE

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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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