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FDA 510(k)

REPORT AND IMAGE MANAGEMENT SYSTEM

K-Number: K882754 · 1988-10-21

ApplicantMedical Image Processing Specialists, Inc.
Decision Date1988-10-21
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REPORT AND IMAGE MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Image Processing Specialists, Inc.. It received FDA 510(k) clearance on 1988-10-21 under 510(k) number K882754. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPORT AND IMAGE MANAGEMENT SYSTEM?

REPORT AND IMAGE MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1988-10-21. The listed applicant is Medical Image Processing Specialists, Inc.. The 510(k) number is K882754.

When did REPORT AND IMAGE MANAGEMENT SYSTEM receive FDA 510(k) clearance?

REPORT AND IMAGE MANAGEMENT SYSTEM received FDA 510(k) clearance on 1988-10-21, under 510(k) number K882754.

Who is the listed applicant for REPORT AND IMAGE MANAGEMENT SYSTEM?

The FDA 510(k) record lists Medical Image Processing Specialists, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPORT AND IMAGE MANAGEMENT SYSTEM?

The FDA product code for REPORT AND IMAGE MANAGEMENT SYSTEM is LMD.

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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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