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FDA 510(k)

URITEST 9, INLAB REAGENT STRIPS URINALY

K-Number: K822709 · 1983-01-28

ApplicantLaprol Scientific, Inc.
Decision Date1983-01-28
Product CodeJMA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URITEST 9, INLAB REAGENT STRIPS URINALY 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 1983-01-28 under 510(k) number K822709. The device is classified under product code JMA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URITEST 9, INLAB REAGENT STRIPS URINALY?

URITEST 9, INLAB REAGENT STRIPS URINALY is a medical device that received FDA 510(k) clearance on 1983-01-28. The listed applicant is Laprol Scientific, Inc.. The 510(k) number is K822709.

When did URITEST 9, INLAB REAGENT STRIPS URINALY receive FDA 510(k) clearance?

URITEST 9, INLAB REAGENT STRIPS URINALY received FDA 510(k) clearance on 1983-01-28, under 510(k) number K822709.

Who is the listed applicant for URITEST 9, INLAB REAGENT STRIPS URINALY?

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 URITEST 9, INLAB REAGENT STRIPS URINALY?

The FDA product code for URITEST 9, INLAB REAGENT STRIPS URINALY is JMA.

Related Clinical Trials

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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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.

K831498URI-TEST 3, INLAB REAGENT STRIPS-URINALK831499GLUCOSE 3, INLAB REAGENT STRIPS-URINALY

Related Devices (Code: JMA)

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.

K931523QUANTIMETRIX C-CLEAR(TM)Quantimetrix Corp.K830978HELENA BIOSTRIP AHelena Laboratories

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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