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FDA 510(k)

COMPUMED DICON CLIENT

K-Number: K955708 · 1996-03-01

ApplicantCompumed, Inc.
Decision Date1996-03-01
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPUMED DICON CLIENT is the device name listed in this FDA 510(k) record. The listed applicant is Compumed, Inc.. It received FDA 510(k) clearance on 1996-03-01 under 510(k) number K955708. 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 COMPUMED DICON CLIENT?

COMPUMED DICON CLIENT is a medical device that received FDA 510(k) clearance on 1996-03-01. The listed applicant is Compumed, Inc.. The 510(k) number is K955708.

When did COMPUMED DICON CLIENT receive FDA 510(k) clearance?

COMPUMED DICON CLIENT received FDA 510(k) clearance on 1996-03-01, under 510(k) number K955708.

Who is the listed applicant for COMPUMED DICON CLIENT?

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

What is the FDA product code for COMPUMED DICON CLIENT?

The FDA product code for COMPUMED DICON CLIENT is LMD.

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Other records listing Compumed, 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.

K984285OSTEOGRAM BONE DENSITOMETERK863965KENZ-ECG 102K854626COMPUMED PULMONARY FUNCTION ANALYZER MODEL 307BK802272COMPUTER ECG TERMINALK771648COMPUTER ECG TERMINAL

Related Devices (Code: LMD)

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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Official Source

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