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FDA 510(k)

SHANGHAI GANGHAI MODEL GIKO 1400

K-Number: K063334 · 2006-12-08

ApplicantShanghai Gangkai Purifying Products Co., Ltd.
Decision Date2006-12-08
Product CodeMSH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHANGHAI GANGHAI MODEL GIKO 1400 is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Gangkai Purifying Products Co., Ltd.. It received FDA 510(k) clearance on 2006-12-08 under 510(k) number K063334. The device is classified under product code MSH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHANGHAI GANGHAI MODEL GIKO 1400?

SHANGHAI GANGHAI MODEL GIKO 1400 is a medical device that received FDA 510(k) clearance on 2006-12-08. The listed applicant is Shanghai Gangkai Purifying Products Co., Ltd.. The 510(k) number is K063334.

When did SHANGHAI GANGHAI MODEL GIKO 1400 receive FDA 510(k) clearance?

SHANGHAI GANGHAI MODEL GIKO 1400 received FDA 510(k) clearance on 2006-12-08, under 510(k) number K063334.

Who is the listed applicant for SHANGHAI GANGHAI MODEL GIKO 1400?

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

What is the FDA product code for SHANGHAI GANGHAI MODEL GIKO 1400?

The FDA product code for SHANGHAI GANGHAI MODEL GIKO 1400 is MSH.

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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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