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FDA 510(k)

CATHETER, SAMPLING, CONDUIT

K-Number: K771066 · 1977-07-11

ApplicantMentor Corp.
Decision Date1977-07-11
Product CodeFEZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER, SAMPLING, CONDUIT is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1977-07-11 under 510(k) number K771066. The device is classified under product code FEZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, SAMPLING, CONDUIT?

CATHETER, SAMPLING, CONDUIT is a medical device that received FDA 510(k) clearance on 1977-07-11. The listed applicant is Mentor Corp.. The 510(k) number is K771066.

When did CATHETER, SAMPLING, CONDUIT receive FDA 510(k) clearance?

CATHETER, SAMPLING, CONDUIT received FDA 510(k) clearance on 1977-07-11, under 510(k) number K771066.

Who is the listed applicant for CATHETER, SAMPLING, CONDUIT?

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 CATHETER, SAMPLING, CONDUIT?

The FDA product code for CATHETER, SAMPLING, CONDUIT is FEZ.

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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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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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