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FDA 510(k)

MICRO-FOCUS 50 CABINET X-RAY

K-Number: K852634 · 1985-07-19

ApplicantMicro-Focus Imaging., Inc.
Decision Date1985-07-19
Product CodeMWP
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICRO-FOCUS 50 CABINET X-RAY 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 1985-07-19 under 510(k) number K852634. The device is classified under product code MWP. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-FOCUS 50 CABINET X-RAY?

MICRO-FOCUS 50 CABINET X-RAY is a medical device that received FDA 510(k) clearance on 1985-07-19. The listed applicant is Micro-Focus Imaging., Inc.. The 510(k) number is K852634.

When did MICRO-FOCUS 50 CABINET X-RAY receive FDA 510(k) clearance?

MICRO-FOCUS 50 CABINET X-RAY received FDA 510(k) clearance on 1985-07-19, under 510(k) number K852634.

Who is the listed applicant for MICRO-FOCUS 50 CABINET X-RAY?

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 MICRO-FOCUS 50 CABINET X-RAY?

The FDA product code for MICRO-FOCUS 50 CABINET X-RAY is MWP.

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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 100/30K926434SIS-300(N)-DIA SCAN

Related Devices (Code: MWP)

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.

K230140TrueView Core 100Pro-US Core Specimen Radiography System (TrueView Core 100Pro-US)Compai Healthcare (Suzhou) Co.,LtdK230136TrueView 200 Pro-US Specimen Radiography System (TrueView 200 Pro-US)Compai Healthcare (Suzhou) Co.,LtdK213691Solas ORCirdan Imaging, Ltd.K210955Kubtec Mozart Supra (XPERT 84) Radiography SystemKub Technologies, Inc.K210956Kubtec Mozart (XPERT42)Kub Technologies, Inc.K210957Kubec Xpert 80 Radiography SystemKub Technologies, Inc.

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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