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)

LASERNET IMAGE MANAGER/PRINT SERVER

K-Number: K952485 · 1995-11-24

ApplicantFrantz Imaging, Inc.
Decision Date1995-11-24
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LASERNET IMAGE MANAGER/PRINT SERVER is the device name listed in this FDA 510(k) record. The listed applicant is Frantz Imaging, Inc.. It received FDA 510(k) clearance on 1995-11-24 under 510(k) number K952485. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASERNET IMAGE MANAGER/PRINT SERVER?

LASERNET IMAGE MANAGER/PRINT SERVER is a medical device that received FDA 510(k) clearance on 1995-11-24. The listed applicant is Frantz Imaging, Inc.. The 510(k) number is K952485.

When did LASERNET IMAGE MANAGER/PRINT SERVER receive FDA 510(k) clearance?

LASERNET IMAGE MANAGER/PRINT SERVER received FDA 510(k) clearance on 1995-11-24, under 510(k) number K952485.

Who is the listed applicant for LASERNET IMAGE MANAGER/PRINT SERVER?

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

What is the FDA product code for LASERNET IMAGE MANAGER/PRINT SERVER?

The FDA product code for LASERNET IMAGE MANAGER/PRINT SERVER is LMA.

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 Frantz Imaging, 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.

K921215LASERSTAR IMAGERK871957SPACEMISER 8-10 FILM RECORDERK871958SPACEMISER 8-17 FILM RECORDERK871959FRANTZ IMAGING COMPACT CAMERA

Related Devices (Code: LMA)

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.

K132183DICOM VIDEOBar Code Computer, Ltd.K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDVidar Systems Corp.K130406DIAGNOSTICPRO EDGEVidar Systems Corp.K102476TELERADPROVidar Systems Corp.K093809VIDAR DENTAL FILM DIGITIZERVidar Systems Corp.K091288MEDI-6000 MEDICAL IMAGE DIGITIZERMicrotek International, 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.

↑