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FDA 510(k)

MINI IMAGER

K-Number: K950423 · 1995-05-12

ApplicantRegulatory Management Services
Decision Date1995-05-12
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MINI IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is Regulatory Management Services. It received FDA 510(k) clearance on 1995-05-12 under 510(k) number K950423. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI IMAGER?

MINI IMAGER is a medical device that received FDA 510(k) clearance on 1995-05-12. The listed applicant is Regulatory Management Services. The 510(k) number is K950423.

When did MINI IMAGER receive FDA 510(k) clearance?

MINI IMAGER received FDA 510(k) clearance on 1995-05-12, under 510(k) number K950423.

Who is the listed applicant for MINI IMAGER?

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

What is the FDA product code for MINI IMAGER?

The FDA product code for MINI IMAGER is LMC.

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Other records listing Regulatory Management Services 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.

K070907INTERSON USB ULTRASOUND PROBE SYSTEMK950699PREVIEW TELEIMAGING SYSTEM

Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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.

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