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FDA 510(k)

YESNG SUPER FRECATOR

K-Number: K882903 · 1988-07-28

ApplicantFerguson Medical
Decision Date1988-07-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YESNG SUPER FRECATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K882903. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YESNG SUPER FRECATOR?

YESNG SUPER FRECATOR is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Ferguson Medical. The 510(k) number is K882903.

When did YESNG SUPER FRECATOR receive FDA 510(k) clearance?

YESNG SUPER FRECATOR received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882903.

Who is the listed applicant for YESNG SUPER FRECATOR?

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

What is the FDA product code for YESNG SUPER FRECATOR?

The FDA product code for YESNG SUPER FRECATOR is GEI.

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Other records listing Ferguson Medical as applicant

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Related Devices (Code: GEI)

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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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