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)

DELTASCAN 2060 CT SCANNER

K-Number: K812410 · 1981-10-02

ApplicantTechnicare Corp.
Decision Date1981-10-02
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DELTASCAN 2060 CT SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1981-10-02 under 510(k) number K812410. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTASCAN 2060 CT SCANNER?

DELTASCAN 2060 CT SCANNER is a medical device that received FDA 510(k) clearance on 1981-10-02. The listed applicant is Technicare Corp.. The 510(k) number is K812410.

When did DELTASCAN 2060 CT SCANNER receive FDA 510(k) clearance?

DELTASCAN 2060 CT SCANNER received FDA 510(k) clearance on 1981-10-02, under 510(k) number K812410.

Who is the listed applicant for DELTASCAN 2060 CT SCANNER?

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

What is the FDA product code for DELTASCAN 2060 CT SCANNER?

The FDA product code for DELTASCAN 2060 CT SCANNER is JAK.

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 Technicare Corp. 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.

K854340TECHNICARE 720 HPS CT SCANNERK852089SATURN NUCLEAR MEDICINE COMPUTER SYSTEMK844293AUTO DII MULTI FREQUENCYK844247ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMSK843716NUCLEAR 700 MEDICINE MECHANICAL POSIT-K842777AUTOFOCUS DUAL ELEMENT PROBE

View all 32 devices →

Related Devices (Code: JAK)

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.

K261125BodyTom 64 (NL4100); OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA View Phase 6.0Fujifilm CorporationK253836FCT iStream Phase 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, LLC

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.

↑