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FDA 510(k)

ASPECT DIGITAL FORMATTER

K-Number: K954149 · 1995-11-13

ApplicantAspect Electronics, Inc.
Decision Date1995-11-13
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ASPECT DIGITAL FORMATTER is the device name listed in this FDA 510(k) record. The listed applicant is Aspect Electronics, Inc.. It received FDA 510(k) clearance on 1995-11-13 under 510(k) number K954149. 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 ASPECT DIGITAL FORMATTER?

ASPECT DIGITAL FORMATTER is a medical device that received FDA 510(k) clearance on 1995-11-13. The listed applicant is Aspect Electronics, Inc.. The 510(k) number is K954149.

When did ASPECT DIGITAL FORMATTER receive FDA 510(k) clearance?

ASPECT DIGITAL FORMATTER received FDA 510(k) clearance on 1995-11-13, under 510(k) number K954149.

Who is the listed applicant for ASPECT DIGITAL FORMATTER?

The FDA 510(k) record lists Aspect Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASPECT DIGITAL FORMATTER?

The FDA product code for ASPECT DIGITAL FORMATTER is LMC.

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.

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Other records listing Aspect Electronics, 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.

K962051ASPECT OPTICAMK954875ASPECT ACQUISITION MODULE (AAM)

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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