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FDA 510(k)

MENTOR ALLOPLASTIC SPERMATOCELE

K-Number: K863565 · 1986-11-19

ApplicantMentor Corp.
Decision Date1986-11-19
Product CodeLQS
DecisionSubstantially Equivalent

Device Summary

MENTOR ALLOPLASTIC SPERMATOCELE is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K863565. The device is classified under product code LQS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR ALLOPLASTIC SPERMATOCELE?

MENTOR ALLOPLASTIC SPERMATOCELE is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Mentor Corp.. The 510(k) number is K863565.

When did MENTOR ALLOPLASTIC SPERMATOCELE receive FDA 510(k) clearance?

MENTOR ALLOPLASTIC SPERMATOCELE received FDA 510(k) clearance on 1986-11-19, under 510(k) number K863565.

Who is the listed applicant for MENTOR ALLOPLASTIC SPERMATOCELE?

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 ALLOPLASTIC SPERMATOCELE?

The FDA product code for MENTOR ALLOPLASTIC SPERMATOCELE is LQS.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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