FDA 510(k)

E. CAM PROFILE ATTENUATION CORRECTION

K-Number: K963983 · 1997-03-31

Decision Date1997-03-31

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

E. CAM PROFILE ATTENUATION CORRECTION is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1997-03-31 under 510(k) number K963983. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E. CAM PROFILE ATTENUATION CORRECTION?

E. CAM PROFILE ATTENUATION CORRECTION is a medical device that received FDA 510(k) clearance on 1997-03-31. The listed applicant is Siemens Corp.. The 510(k) number is K963983.

When did E. CAM PROFILE ATTENUATION CORRECTION receive FDA 510(k) clearance?

E. CAM PROFILE ATTENUATION CORRECTION received FDA 510(k) clearance on 1997-03-31, under 510(k) number K963983.

Who is the listed applicant for E. CAM PROFILE ATTENUATION CORRECTION?

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

What is the FDA product code for E. CAM PROFILE ATTENUATION CORRECTION?

The FDA product code for E. CAM PROFILE ATTENUATION CORRECTION is KPS.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Siemens Corp. as applicant

K103360DIMENSION VISTA DIGITOXIN CALIBRATOR - DGTX CAL K993947KOORDINANT ANGIOGRAPHIC AND OPERATING ROOM MODEL X-RAY TABLE FAMILY K992925AX WORKSTATION DR-VIEWER SOFTWARE OPTION K991652HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM K991600SOMATOM PLUS 4 WITH SLIDING GANTRY OPTION K984221FUNCTIONAL MRI PACKAGE FOR MAGETETOM VISION MR

View all 66 devices →

Related Devices (Code: KPS)

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.