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FDA 510(k)

SHANCHUAN SYRINGE

K-Number: K021993 · 2003-06-03

ApplicantShangdong Zibo Shanchuan Medical Instruments Co.
Decision Date2003-06-03
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHANCHUAN SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Shangdong Zibo Shanchuan Medical Instruments Co.. It received FDA 510(k) clearance on 2003-06-03 under 510(k) number K021993. 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 SHANCHUAN SYRINGE?

SHANCHUAN SYRINGE is a medical device that received FDA 510(k) clearance on 2003-06-03. The listed applicant is Shangdong Zibo Shanchuan Medical Instruments Co.. The 510(k) number is K021993.

When did SHANCHUAN SYRINGE receive FDA 510(k) clearance?

SHANCHUAN SYRINGE received FDA 510(k) clearance on 2003-06-03, under 510(k) number K021993.

Who is the listed applicant for SHANCHUAN SYRINGE?

The FDA 510(k) record lists Shangdong Zibo Shanchuan Medical Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHANCHUAN SYRINGE?

The FDA product code for SHANCHUAN SYRINGE is FMF.

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Other records listing Shangdong Zibo Shanchuan Medical Instruments Co. as applicant

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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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