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FDA 510(k)

YUSHENG DISPOSABLE VAGINAL SPECULUM

K-Number: K052912 · 2005-12-15

Decision Date2005-12-15
Product CodeHIB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

YUSHENG DISPOSABLE VAGINAL SPECULUM is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Yusheng Medical Instrument Co. , Ltd.. It received FDA 510(k) clearance on 2005-12-15 under 510(k) number K052912. The device is classified under product code HIB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YUSHENG DISPOSABLE VAGINAL SPECULUM?

YUSHENG DISPOSABLE VAGINAL SPECULUM is a medical device that received FDA 510(k) clearance on 2005-12-15. The listed applicant is Zhejiang Yusheng Medical Instrument Co. , Ltd.. The 510(k) number is K052912.

When did YUSHENG DISPOSABLE VAGINAL SPECULUM receive FDA 510(k) clearance?

YUSHENG DISPOSABLE VAGINAL SPECULUM received FDA 510(k) clearance on 2005-12-15, under 510(k) number K052912.

Who is the listed applicant for YUSHENG DISPOSABLE VAGINAL SPECULUM?

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

What is the FDA product code for YUSHENG DISPOSABLE VAGINAL SPECULUM?

The FDA product code for YUSHENG DISPOSABLE VAGINAL SPECULUM is HIB.

Related Clinical Trials

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.

Related Devices (Code: HIB)

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.

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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