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FDA 510(k)

YESNG PATIENT PLATE #80226

K-Number: K881144 · 1988-04-08

ApplicantFerguson Medical
Decision Date1988-04-08
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YESNG PATIENT PLATE #80226 is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-04-08 under 510(k) number K881144. The device is classified under product code JOS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YESNG PATIENT PLATE #80226?

YESNG PATIENT PLATE #80226 is a medical device that received FDA 510(k) clearance on 1988-04-08. The listed applicant is Ferguson Medical. The 510(k) number is K881144.

When did YESNG PATIENT PLATE #80226 receive FDA 510(k) clearance?

YESNG PATIENT PLATE #80226 received FDA 510(k) clearance on 1988-04-08, under 510(k) number K881144.

Who is the listed applicant for YESNG PATIENT PLATE #80226?

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 PATIENT PLATE #80226?

The FDA product code for YESNG PATIENT PLATE #80226 is JOS.

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Other records listing Ferguson Medical as applicant

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Related Devices (Code: JOS)

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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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