FDA 510(k)

MULTISPECT 2 511 KEV COLLIMATOR

K-Number: K972360 · 1997-09-23

ApplicantSiemens Medical Solutions USA, Inc.

Decision Date1997-09-23

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MULTISPECT 2 511 KEV COLLIMATOR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1997-09-23 under 510(k) number K972360. 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 MULTISPECT 2 511 KEV COLLIMATOR?

MULTISPECT 2 511 KEV COLLIMATOR is a medical device that received FDA 510(k) clearance on 1997-09-23. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K972360.

When did MULTISPECT 2 511 KEV COLLIMATOR receive FDA 510(k) clearance?

MULTISPECT 2 511 KEV COLLIMATOR received FDA 510(k) clearance on 1997-09-23, under 510(k) number K972360.

Who is the listed applicant for MULTISPECT 2 511 KEV COLLIMATOR?

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

What is the FDA product code for MULTISPECT 2 511 KEV COLLIMATOR?

The FDA product code for MULTISPECT 2 511 KEV COLLIMATOR 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

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.