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FDA 510(k)

BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES

K-Number: K083686 · 2009-07-02

ApplicantAnhui Kangda Medical Products Co., Ltd.
Decision Date2009-07-02
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Kangda Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2009-07-02 under 510(k) number K083686. 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 BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES?

BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES is a medical device that received FDA 510(k) clearance on 2009-07-02. The listed applicant is Anhui Kangda Medical Products Co., Ltd.. The 510(k) number is K083686.

When did BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES receive FDA 510(k) clearance?

BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES received FDA 510(k) clearance on 2009-07-02, under 510(k) number K083686.

Who is the listed applicant for BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES?

The FDA 510(k) record lists Anhui Kangda Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES?

The FDA product code for BAIXIN DISPOSABLE SYRINGE, MULTIPLE SIZES is FMF.

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Other records listing Anhui Kangda Medical Products Co., Ltd. as applicant

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.

K083687BAIXIN INTRAVASCULAR ADMINISTRATION SET

Related Devices (Code: FMF)

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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