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FDA 510(k)

SHANG HO

K-Number: K970795 · 1997-12-18

ApplicantShang HO Industrial Corp. , Ltd.
Decision Date1997-12-18
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHANG HO is the device name listed in this FDA 510(k) record. The listed applicant is Shang HO Industrial Corp. , Ltd.. It received FDA 510(k) clearance on 1997-12-18 under 510(k) number K970795. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHANG HO?

SHANG HO is a medical device that received FDA 510(k) clearance on 1997-12-18. The listed applicant is Shang HO Industrial Corp. , Ltd.. The 510(k) number is K970795.

When did SHANG HO receive FDA 510(k) clearance?

SHANG HO received FDA 510(k) clearance on 1997-12-18, under 510(k) number K970795.

Who is the listed applicant for SHANG HO?

The FDA 510(k) record lists Shang HO Industrial Corp. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHANG HO?

The FDA product code for SHANG HO is KGO.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Shang HO Industrial Corp. , 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.

K964819SHENG HO

Related Devices (Code: KGO)

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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