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FDA 510(k)

SHANGRING

K-Number: K131373 · 2013-06-25

ApplicantWuhu Snnda Medical Treatment Appliance Technology
Decision Date2013-06-25
Product CodeHFX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SHANGRING is the device name listed in this FDA 510(k) record. The listed applicant is Wuhu Snnda Medical Treatment Appliance Technology. It received FDA 510(k) clearance on 2013-06-25 under 510(k) number K131373. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHANGRING?

SHANGRING is a medical device that received FDA 510(k) clearance on 2013-06-25. The listed applicant is Wuhu Snnda Medical Treatment Appliance Technology. The 510(k) number is K131373.

When did SHANGRING receive FDA 510(k) clearance?

SHANGRING received FDA 510(k) clearance on 2013-06-25, under 510(k) number K131373.

Who is the listed applicant for SHANGRING?

The FDA 510(k) record lists Wuhu Snnda Medical Treatment Appliance Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHANGRING?

The FDA product code for SHANGRING is HFX.

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.

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Related Devices (Code: HFX)

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.

K251687Konig Bell Circumcision ClampMedline Industries, LPK221356Wee BellWee MedicalK212911Konig Mogen ClampMedline Industries, Inc.K121789SHANGRINGWuhu Snna Medical Treatment Appliance Technology CK103695PREPEX SYSTEMCirc MedtechK100916MEDICON MOGEN CLAMPMedicon EG

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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