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)

COLLIMARE COLLIMATOR FAMILY

K-Number: K073124 · 2007-11-16

ApplicantCollimare, LLC
Decision Date2007-11-16
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLLIMARE COLLIMATOR FAMILY is the device name listed in this FDA 510(k) record. The listed applicant is Collimare, LLC. It received FDA 510(k) clearance on 2007-11-16 under 510(k) number K073124. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLIMARE COLLIMATOR FAMILY?

COLLIMARE COLLIMATOR FAMILY is a medical device that received FDA 510(k) clearance on 2007-11-16. The listed applicant is Collimare, LLC. The 510(k) number is K073124.

When did COLLIMARE COLLIMATOR FAMILY receive FDA 510(k) clearance?

COLLIMARE COLLIMATOR FAMILY received FDA 510(k) clearance on 2007-11-16, under 510(k) number K073124.

Who is the listed applicant for COLLIMARE COLLIMATOR FAMILY?

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

What is the FDA product code for COLLIMARE COLLIMATOR FAMILY?

The FDA product code for COLLIMARE COLLIMATOR FAMILY is IZW.

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

Related Devices (Code: IZW)

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.

K101039SHIMADZU COLLIMATOR R-300Shimadzu Corp.K093572R650 QDASM COLLIMATOROmega Medical Imaging, Inc.K090578SHIMADZU COLLIMATOR R-30HShimadzu Corp.K091517RALCO, MODEL R225 ACSRalco S.R.L.K083029MODEL R605DASM AUTOMATIC X-RAY COLLIMATORRalco S.R.L.K072780MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATORRalco S.R.L.

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.

↑