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FDA 510(k)

SIS-300(N)-DIA SCAN

K-Number: K926434 · 1993-03-18

ApplicantMicro-Focus Imaging., Inc.
Decision Date1993-03-18
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIS-300(N)-DIA SCAN is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Focus Imaging., Inc.. It received FDA 510(k) clearance on 1993-03-18 under 510(k) number K926434. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIS-300(N)-DIA SCAN?

SIS-300(N)-DIA SCAN is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is Micro-Focus Imaging., Inc.. The 510(k) number is K926434.

When did SIS-300(N)-DIA SCAN receive FDA 510(k) clearance?

SIS-300(N)-DIA SCAN received FDA 510(k) clearance on 1993-03-18, under 510(k) number K926434.

Who is the listed applicant for SIS-300(N)-DIA SCAN?

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

What is the FDA product code for SIS-300(N)-DIA SCAN?

The FDA product code for SIS-300(N)-DIA SCAN is JAA.

Other records listing Micro-Focus Imaging., Inc. 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.

K953404OSTEO-RAY 100K953292CP 100/30K852634MICRO-FOCUS 50 CABINET X-RAY

Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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.

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