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)

DIGITAL DILUTER/DISPENSERS

K-Number: K822688 · 1982-11-05

ApplicantHamilton Co.
Decision Date1982-11-05
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIGITAL DILUTER/DISPENSERS is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Co.. It received FDA 510(k) clearance on 1982-11-05 under 510(k) number K822688. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL DILUTER/DISPENSERS?

DIGITAL DILUTER/DISPENSERS is a medical device that received FDA 510(k) clearance on 1982-11-05. The listed applicant is Hamilton Co.. The 510(k) number is K822688.

When did DIGITAL DILUTER/DISPENSERS receive FDA 510(k) clearance?

DIGITAL DILUTER/DISPENSERS received FDA 510(k) clearance on 1982-11-05, under 510(k) number K822688.

Who is the listed applicant for DIGITAL DILUTER/DISPENSERS?

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

What is the FDA product code for DIGITAL DILUTER/DISPENSERS?

The FDA product code for DIGITAL DILUTER/DISPENSERS is JQW.

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 Hamilton 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.

K961896MICROLAB 4000, MICROLAB 4200K943493DISCRETE PHOTOMETRIC CHEMISTRY ANALYZERK892369MULTI-PROBE HEAD PLUSK873893LUMICONK871945MICROLAB ATK832204MICROLAB P

View all 16 devices →

Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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.

↑