FDA 510(k)

FYODOROV RADIAL KERATOTOMY MARKER SET

K-Number: K860329 · 1986-02-12

Decision Date1986-02-12

Product CodeHHR

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

FYODOROV RADIAL KERATOTOMY MARKER SET is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tech Develoment Corp.. It received FDA 510(k) clearance on 1986-02-12 under 510(k) number K860329. The device is classified under product code HHR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FYODOROV RADIAL KERATOTOMY MARKER SET?

FYODOROV RADIAL KERATOTOMY MARKER SET is a medical device that received FDA 510(k) clearance on 1986-02-12. The listed applicant is Med-Tech Develoment Corp.. The 510(k) number is K860329.

When did FYODOROV RADIAL KERATOTOMY MARKER SET receive FDA 510(k) clearance?

FYODOROV RADIAL KERATOTOMY MARKER SET received FDA 510(k) clearance on 1986-02-12, under 510(k) number K860329.

Who is the listed applicant for FYODOROV RADIAL KERATOTOMY MARKER SET?

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

What is the FDA product code for FYODOROV RADIAL KERATOTOMY MARKER SET?

The FDA product code for FYODOROV RADIAL KERATOTOMY MARKER SET is HHR.

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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.