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FDA 510(k)

LANCER URIC ACID AUTO/STAT KIT

K-Number: K802692 · 1980-12-10

ApplicantSherwood Medical Co.
Decision Date1980-12-10
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LANCER URIC ACID AUTO/STAT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1980-12-10 under 510(k) number K802692. 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 LANCER URIC ACID AUTO/STAT KIT?

LANCER URIC ACID AUTO/STAT KIT is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is Sherwood Medical Co.. The 510(k) number is K802692.

When did LANCER URIC ACID AUTO/STAT KIT receive FDA 510(k) clearance?

LANCER URIC ACID AUTO/STAT KIT received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802692.

Who is the listed applicant for LANCER URIC ACID AUTO/STAT KIT?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LANCER URIC ACID AUTO/STAT KIT?

The FDA product code for LANCER URIC ACID AUTO/STAT KIT is KNK.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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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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