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FDA 510(k)

CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS

K-Number: K030690 · 2003-04-30

Decision Date2003-04-30
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS is the device name listed in this FDA 510(k) record. The listed applicant is Codonics, Inc.. It received FDA 510(k) clearance on 2003-04-30 under 510(k) number K030690. 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 CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS?

CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS is a medical device that received FDA 510(k) clearance on 2003-04-30. The listed applicant is Codonics, Inc.. The 510(k) number is K030690.

When did CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS receive FDA 510(k) clearance?

CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS received FDA 510(k) clearance on 2003-04-30, under 510(k) number K030690.

Who is the listed applicant for CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS?

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

What is the FDA product code for CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS?

The FDA product code for CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS 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.

Other records listing Codonics, 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.

View all 7 devices →

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.

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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