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FDA 510(k)

GOLDEN SPYDER, MODEL GS-300

K-Number: K041341 · 2004-06-03

ApplicantGolden Technologies, Inc.
Decision Date2004-06-03
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GOLDEN SPYDER, MODEL GS-300 is the device name listed in this FDA 510(k) record. The listed applicant is Golden Technologies, Inc.. It received FDA 510(k) clearance on 2004-06-03 under 510(k) number K041341. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOLDEN SPYDER, MODEL GS-300?

GOLDEN SPYDER, MODEL GS-300 is a medical device that received FDA 510(k) clearance on 2004-06-03. The listed applicant is Golden Technologies, Inc.. The 510(k) number is K041341.

When did GOLDEN SPYDER, MODEL GS-300 receive FDA 510(k) clearance?

GOLDEN SPYDER, MODEL GS-300 received FDA 510(k) clearance on 2004-06-03, under 510(k) number K041341.

Who is the listed applicant for GOLDEN SPYDER, MODEL GS-300?

The FDA 510(k) record lists Golden Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GOLDEN SPYDER, MODEL GS-300?

The FDA product code for GOLDEN SPYDER, MODEL GS-300 is ITI.

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Other records listing Golden Technologies, Inc. as applicant

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Related Devices (Code: ITI)

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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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