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FDA 510(k)

TELEMEDIC TELERADIOLOGY SYSTEM

K-Number: K921185 · 1993-03-29

ApplicantMeditron Corp.
Decision Date1993-03-29
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TELEMEDIC TELERADIOLOGY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Meditron Corp.. It received FDA 510(k) clearance on 1993-03-29 under 510(k) number K921185. 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 TELEMEDIC TELERADIOLOGY SYSTEM?

TELEMEDIC TELERADIOLOGY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-29. The listed applicant is Meditron Corp.. The 510(k) number is K921185.

When did TELEMEDIC TELERADIOLOGY SYSTEM receive FDA 510(k) clearance?

TELEMEDIC TELERADIOLOGY SYSTEM received FDA 510(k) clearance on 1993-03-29, under 510(k) number K921185.

Who is the listed applicant for TELEMEDIC TELERADIOLOGY SYSTEM?

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

What is the FDA product code for TELEMEDIC TELERADIOLOGY SYSTEM?

The FDA product code for TELEMEDIC TELERADIOLOGY 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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