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FDA 510(k)

PURECARE AT-903 T.E.N.S.

K-Number: K931715 · 1994-01-27

ApplicantFuching Enterprise Co., Ltd.
Decision Date1994-01-27
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PURECARE AT-903 T.E.N.S. is the device name listed in this FDA 510(k) record. The listed applicant is Fuching Enterprise Co., Ltd.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K931715. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PURECARE AT-903 T.E.N.S.?

PURECARE AT-903 T.E.N.S. is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Fuching Enterprise Co., Ltd.. The 510(k) number is K931715.

When did PURECARE AT-903 T.E.N.S. receive FDA 510(k) clearance?

PURECARE AT-903 T.E.N.S. received FDA 510(k) clearance on 1994-01-27, under 510(k) number K931715.

Who is the listed applicant for PURECARE AT-903 T.E.N.S.?

The FDA 510(k) record lists Fuching Enterprise Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PURECARE AT-903 T.E.N.S.?

The FDA product code for PURECARE AT-903 T.E.N.S. is GZJ.

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Related Devices (Code: GZJ)

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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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