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FDA 510(k)

UROPAPER EIKEN AG

K-Number: K932365 · 1993-11-26

ApplicantTanabe U.S.A., Inc.
Decision Date1993-11-26
Product CodeJIL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UROPAPER EIKEN AG is the device name listed in this FDA 510(k) record. The listed applicant is Tanabe U.S.A., Inc.. It received FDA 510(k) clearance on 1993-11-26 under 510(k) number K932365. The device is classified under product code JIL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROPAPER EIKEN AG?

UROPAPER EIKEN AG is a medical device that received FDA 510(k) clearance on 1993-11-26. The listed applicant is Tanabe U.S.A., Inc.. The 510(k) number is K932365.

When did UROPAPER EIKEN AG receive FDA 510(k) clearance?

UROPAPER EIKEN AG received FDA 510(k) clearance on 1993-11-26, under 510(k) number K932365.

Who is the listed applicant for UROPAPER EIKEN AG?

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

What is the FDA product code for UROPAPER EIKEN AG?

The FDA product code for UROPAPER EIKEN AG is JIL.

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Other records listing Tanabe U.S.A., Inc. 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.

K932368UROPAPER EIKEN 6BK932366UROPAPER EIKEN HAGK932363UROPAPER EIKEN GKK932367UROPAPER EIKEN 8K931897UROPAPERK932369UROPAPER EIKEN 7

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Related Devices (Code: JIL)

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K193514AUTION MAX AX-4060 Urinalysis SystemArkray, Inc.K183432cobas u 601 urinalysis test systemRoche DiagnosticsK173327DIP/U.S. Urine Analysis Test SystemHealthy.Io, Ltd.K180356inui In-Home Urine Analysis Test SystemScanadu, Inc.K181024DUS 2GP Reagent Strips, DUS 5 Reagent Strips, DUS 10 Reagent StripsDFI Co., Ltd.K171521DUS R-50S (Urine Chemistry system)DFI Co., Ltd.

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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