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)

NP-2600 SERIES HARDCOPY PRINTERS

K-Number: K042232 · 2004-10-05

ApplicantCodonics, Inc.
Decision Date2004-10-05
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NP-2600 SERIES HARDCOPY PRINTERS is the device name listed in this FDA 510(k) record. The listed applicant is Codonics, Inc.. It received FDA 510(k) clearance on 2004-10-05 under 510(k) number K042232. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NP-2600 SERIES HARDCOPY PRINTERS?

NP-2600 SERIES HARDCOPY PRINTERS is a medical device that received FDA 510(k) clearance on 2004-10-05. The listed applicant is Codonics, Inc.. The 510(k) number is K042232.

When did NP-2600 SERIES HARDCOPY PRINTERS receive FDA 510(k) clearance?

NP-2600 SERIES HARDCOPY PRINTERS received FDA 510(k) clearance on 2004-10-05, under 510(k) number K042232.

Who is the listed applicant for NP-2600 SERIES HARDCOPY PRINTERS?

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

What is the FDA product code for NP-2600 SERIES HARDCOPY PRINTERS?

The FDA product code for NP-2600 SERIES HARDCOPY PRINTERS is LMC.

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 Codonics, Inc. 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.

K101439CODONICS SAFE LABELING SYSTEM (SLS), MODEL 500I/500PK060440CODONICS HORIZON XL DIGITAL DIRECT LONG FILM IMAGER; CODONICS HORIZON XL-X LONG FILM IMAGERK030690CODONICS EP-1000 MEDICAL COLOR DRY IMAGERSK021054CODONICS HORIZON CI MEDICAL MULTIMEDIA DRY IMAGER; CODONICS HORIZON GS MEDICAL MULTIMEDIA GREY SCALE DRY IMAGERK003481CODONICS NP-1660 SERIES MEDICAL PRINTERS, MODEL 1660K962364CODONICS MEDICAL PRINTER (NP-1600M,NP1600MD)

View all 7 devices →

Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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.

↑