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FDA 510(k)

URI-TEST 3, INLAB REAGENT STRIPS-URINAL

K-Number: K831498 · 1983-06-22

ApplicantLaprol Scientific, Inc.
Decision Date1983-06-22
Product CodeJIL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URI-TEST 3, INLAB REAGENT STRIPS-URINAL is the device name listed in this FDA 510(k) record. The listed applicant is Laprol Scientific, Inc.. It received FDA 510(k) clearance on 1983-06-22 under 510(k) number K831498. 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 URI-TEST 3, INLAB REAGENT STRIPS-URINAL?

URI-TEST 3, INLAB REAGENT STRIPS-URINAL is a medical device that received FDA 510(k) clearance on 1983-06-22. The listed applicant is Laprol Scientific, Inc.. The 510(k) number is K831498.

When did URI-TEST 3, INLAB REAGENT STRIPS-URINAL receive FDA 510(k) clearance?

URI-TEST 3, INLAB REAGENT STRIPS-URINAL received FDA 510(k) clearance on 1983-06-22, under 510(k) number K831498.

Who is the listed applicant for URI-TEST 3, INLAB REAGENT STRIPS-URINAL?

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

What is the FDA product code for URI-TEST 3, INLAB REAGENT STRIPS-URINAL?

The FDA product code for URI-TEST 3, INLAB REAGENT STRIPS-URINAL is JIL.

Related Clinical Trials

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Other records listing Laprol Scientific, 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.

K831499GLUCOSE 3, INLAB REAGENT STRIPS-URINALYK822709URITEST 9, INLAB REAGENT STRIPS URINALY

Related Devices (Code: JIL)

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.

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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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