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FDA 510(k)

COURIER PC

K-Number: K925864 · 1993-09-20

ApplicantShoreline Business Consulting
Decision Date1993-09-20
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COURIER PC is the device name listed in this FDA 510(k) record. The listed applicant is Shoreline Business Consulting. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K925864. 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 COURIER PC?

COURIER PC is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Shoreline Business Consulting. The 510(k) number is K925864.

When did COURIER PC receive FDA 510(k) clearance?

COURIER PC received FDA 510(k) clearance on 1993-09-20, under 510(k) number K925864.

Who is the listed applicant for COURIER PC?

The FDA 510(k) record lists Shoreline Business Consulting as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COURIER PC?

The FDA product code for COURIER PC is LMD.

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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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