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FDA 510(k)

OB-PH - PH TEST PAPER

K-Number: K850858 · 1985-05-24

ApplicantUro Pharmaceuticals, Inc.
Decision Date1985-05-24
Product CodeLNW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

OB-PH - PH TEST PAPER is the device name listed in this FDA 510(k) record. The listed applicant is Uro Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1985-05-24 under 510(k) number K850858. The device is classified under product code LNW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OB-PH - PH TEST PAPER?

OB-PH - PH TEST PAPER is a medical device that received FDA 510(k) clearance on 1985-05-24. The listed applicant is Uro Pharmaceuticals, Inc.. The 510(k) number is K850858.

When did OB-PH - PH TEST PAPER receive FDA 510(k) clearance?

OB-PH - PH TEST PAPER received FDA 510(k) clearance on 1985-05-24, under 510(k) number K850858.

Who is the listed applicant for OB-PH - PH TEST PAPER?

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

What is the FDA product code for OB-PH - PH TEST PAPER?

The FDA product code for OB-PH - PH TEST PAPER is LNW.

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Related Devices (Code: LNW)

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.

K032161PHEM-ALERTFemtek,Llc.K012230PHEM-ALERTFemtek,Llc.K960648PHEM-CHEKFemtek, Inc.

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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