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)

DIGIFLEX AUTOMATIC PIPETTE

K-Number: K830157 · 1983-03-10

ApplicantMicromedic Systems
Decision Date1983-03-10
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIGIFLEX AUTOMATIC PIPETTE is the device name listed in this FDA 510(k) record. The listed applicant is Micromedic Systems. It received FDA 510(k) clearance on 1983-03-10 under 510(k) number K830157. 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 DIGIFLEX AUTOMATIC PIPETTE?

DIGIFLEX AUTOMATIC PIPETTE is a medical device that received FDA 510(k) clearance on 1983-03-10. The listed applicant is Micromedic Systems. The 510(k) number is K830157.

When did DIGIFLEX AUTOMATIC PIPETTE receive FDA 510(k) clearance?

DIGIFLEX AUTOMATIC PIPETTE received FDA 510(k) clearance on 1983-03-10, under 510(k) number K830157.

Who is the listed applicant for DIGIFLEX AUTOMATIC PIPETTE?

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

What is the FDA product code for DIGIFLEX AUTOMATIC PIPETTE?

The FDA product code for DIGIFLEX AUTOMATIC PIPETTE 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 Micromedic Systems 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.

K923643MEDICOOLK872309MICROMEDIC COMBOSTAT LH/FSH KITK870904MICROMEDIC NEONATAL TSH MONOCLONAL IRMA KITK871008MICROMEDIC NEONATAL T4 KITK871505AUTOPAK NEONATAL TSH MONOCLONAL IRMA KITK870245AUTOPAK TSH MONOCLONAL IRMA KIT

View all 42 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.

↑