Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA

K-Number: K023550 · 2002-12-09

ApplicantWiener Laboratories Saic
Decision Date2002-12-09
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA is the device name listed in this FDA 510(k) record. The listed applicant is Wiener Laboratories Saic. It received FDA 510(k) clearance on 2002-12-09 under 510(k) number K023550. The device is classified under product code KNK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA?

WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA is a medical device that received FDA 510(k) clearance on 2002-12-09. The listed applicant is Wiener Laboratories Saic. The 510(k) number is K023550.

When did WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA receive FDA 510(k) clearance?

WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA received FDA 510(k) clearance on 2002-12-09, under 510(k) number K023550.

Who is the listed applicant for WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA?

The FDA 510(k) record lists Wiener Laboratories Saic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA?

The FDA product code for WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA is KNK.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Wiener Laboratories Saic 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.

K023889WIENER LAB. CHAGATEST ELISA RECOMNINANTE V.3.0, MODEL 96 TESTS CAT. NR. 1203254K024305WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006K024116WIENER LAB. BILIRUBINA DIRECT AAK023992WIENER LAB COLINESTERASA AAK023744WIENER LAB. CK-MB DS UV UNITEST, MODEL 28 X 2.5 ML CAT. NR. 1271354K023549WIENER LAB AMILASA 405 AA LIQUIDA

View all 24 devices →

Related Devices (Code: KNK)

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.

K102568URIC ACID MODEL 3P39Abbott LaboratoriesK062862OLYMPUS URIC ACID REAGENT, MODEL OSR6X98Olympus America, Inc.K040467VITALAB URIC ACID REAGENTClinical Data, Inc.K031044ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATORClinical Data, Inc.K022096URIC ACID ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEMBayer Diagnostics Corp.K012038JAS URIC ACID LIQUID REAGENTJas Diagnostics, 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.

↑