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FDA 510(k)

URIDROP SPECIAL

K-Number: K791197 · 1979-07-30

ApplicantAb Medett Produkter
Decision Date1979-07-30
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIDROP SPECIAL is the device name listed in this FDA 510(k) record. The listed applicant is Ab Medett Produkter. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791197. 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 URIDROP SPECIAL?

URIDROP SPECIAL is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Ab Medett Produkter. The 510(k) number is K791197.

When did URIDROP SPECIAL receive FDA 510(k) clearance?

URIDROP SPECIAL received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791197.

Who is the listed applicant for URIDROP SPECIAL?

The FDA 510(k) record lists Ab Medett Produkter as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URIDROP SPECIAL?

The FDA product code for URIDROP SPECIAL 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 Ab Medett Produkter 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.

K791198BIBAGK791196URIDROP

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.K023550WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDAWiener Laboratories Saic

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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