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FDA 510(k)

S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F

K-Number: K984415 · 1999-09-29

ApplicantS.S. White Technologies, Inc.
Decision Date1999-09-29
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F is the device name listed in this FDA 510(k) record. The listed applicant is S.S. White Technologies, Inc.. It received FDA 510(k) clearance on 1999-09-29 under 510(k) number K984415. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F?

S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F is a medical device that received FDA 510(k) clearance on 1999-09-29. The listed applicant is S.S. White Technologies, Inc.. The 510(k) number is K984415.

When did S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F receive FDA 510(k) clearance?

S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F received FDA 510(k) clearance on 1999-09-29, under 510(k) number K984415.

Who is the listed applicant for S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F?

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

What is the FDA product code for S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F?

The FDA product code for S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F is KOJ.

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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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