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)

MULTI-AD FLUID DISPENSING SYSTEM

K-Number: K792227 · 1979-12-20

ApplicantNational Patent Development Corp.
Decision Date1979-12-20
Product CodeKYX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTI-AD FLUID DISPENSING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1979-12-20 under 510(k) number K792227. The device is classified under product code KYX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-AD FLUID DISPENSING SYSTEM?

MULTI-AD FLUID DISPENSING SYSTEM is a medical device that received FDA 510(k) clearance on 1979-12-20. The listed applicant is National Patent Development Corp.. The 510(k) number is K792227.

When did MULTI-AD FLUID DISPENSING SYSTEM receive FDA 510(k) clearance?

MULTI-AD FLUID DISPENSING SYSTEM received FDA 510(k) clearance on 1979-12-20, under 510(k) number K792227.

Who is the listed applicant for MULTI-AD FLUID DISPENSING SYSTEM?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-AD FLUID DISPENSING SYSTEM?

The FDA product code for MULTI-AD FLUID DISPENSING SYSTEM is KYX.

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 National Patent Development Corp. 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.

K843974VARIABLE TEMPERATURE CAUTERY DEVICEK832699HYDRON WOUND DRESSING FAST SEAT KITK822793PIO ROOT CANAL INDICATORK820028ZEON COMPOSITE RESIN LIGHT CURE SYSK820006ZEON COMPOSITE RESIN SYSTEMK811446HYDRON WOUND DRESSING KIT

View all 34 devices →

Related Devices (Code: KYX)

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.

K980109CYCLOTECH CYCLOSPORINE ORAL SOLUTIONS DISPENSERSangstat Medical Corp.K954181CANYONS BI-DIRECTIONAL CHECK VALVECanyon Medical ProductsK830571BOTTLE ADAPTERBurron Medical Products, Inc.K801008MULTI-AD FLUID DISPENSING PUMP MP-3000Burron Medical Products, Inc.K800362FLUID DISPENSING SYSTEMPharmaseal LaboratoriesK800437SYRINGE TIP CONNECTORBurron Medical Products, 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.

↑