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FDA 510(k)

SHENG HO

K-Number: K964819 · 1998-01-06

ApplicantShang HO Industrial Corp. , Ltd.
Decision Date1998-01-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHENG 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 1998-01-06 under 510(k) number K964819. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHENG HO?

SHENG HO is a medical device that received FDA 510(k) clearance on 1998-01-06. The listed applicant is Shang HO Industrial Corp. , Ltd.. The 510(k) number is K964819.

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

SHENG HO received FDA 510(k) clearance on 1998-01-06, under 510(k) number K964819.

Who is the listed applicant for SHENG 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 SHENG HO?

The FDA product code for SHENG HO is LYY.

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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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.

K970795SHANG HO

Related Devices (Code: LYY)

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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