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FDA 510(k)

MENTOR FLAT-SPAN

K-Number: K862049 · 1986-06-10

ApplicantMentor Corp.
Decision Date1986-06-10
Product CodeLCJ
DecisionSubstantially Equivalent

Device Summary

MENTOR FLAT-SPAN is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1986-06-10 under 510(k) number K862049. The device is classified under product code LCJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR FLAT-SPAN?

MENTOR FLAT-SPAN is a medical device that received FDA 510(k) clearance on 1986-06-10. The listed applicant is Mentor Corp.. The 510(k) number is K862049.

When did MENTOR FLAT-SPAN receive FDA 510(k) clearance?

MENTOR FLAT-SPAN received FDA 510(k) clearance on 1986-06-10, under 510(k) number K862049.

Who is the listed applicant for MENTOR FLAT-SPAN?

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 FLAT-SPAN?

The FDA product code for MENTOR FLAT-SPAN is LCJ.

Related Clinical Trials

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.

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.

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Related Devices (Code: LCJ)

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.

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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