FDA 510(k)

SLS-CT

K-Number: K960985 · 1996-10-25

Decision Date1996-10-25

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SLS-CT is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Imaging Research, Inc.. It received FDA 510(k) clearance on 1996-10-25 under 510(k) number K960985. 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 SLS-CT?

SLS-CT is a medical device that received FDA 510(k) clearance on 1996-10-25. The listed applicant is Bio-Imaging Research, Inc.. The 510(k) number is K960985.

When did SLS-CT receive FDA 510(k) clearance?

SLS-CT received FDA 510(k) clearance on 1996-10-25, under 510(k) number K960985.

Who is the listed applicant for SLS-CT?

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

What is the FDA product code for SLS-CT?

The FDA product code for SLS-CT is JAK.

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 Corporation K253836FCT iStream Phase 2Fujifilm Corporation K253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung Company K253770CardIQ SuiteGE Medical Systems SCS K253560Enhanced Boundary for PCCTGe Medical Systems, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.