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FDA 510(k)

YUEFA DISPOSABLE SYRINGE

K-Number: K902178 · 1990-12-21

ApplicantBlue & Red Corp.
Decision Date1990-12-21
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

YUEFA DISPOSABLE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Blue & Red Corp.. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K902178. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YUEFA DISPOSABLE SYRINGE?

YUEFA DISPOSABLE SYRINGE is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Blue & Red Corp.. The 510(k) number is K902178.

When did YUEFA DISPOSABLE SYRINGE receive FDA 510(k) clearance?

YUEFA DISPOSABLE SYRINGE received FDA 510(k) clearance on 1990-12-21, under 510(k) number K902178.

Who is the listed applicant for YUEFA DISPOSABLE SYRINGE?

The FDA 510(k) record lists Blue & Red Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YUEFA DISPOSABLE SYRINGE?

The FDA product code for YUEFA DISPOSABLE SYRINGE is FMF.

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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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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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