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FDA 510(k)

AGFA MODEL CR30-X

K-Number: K062223 · 2006-09-01

ApplicantAgfa Corporation
Decision Date2006-09-01
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AGFA MODEL CR30-X is the device name listed in this FDA 510(k) record. The listed applicant is Agfa Corporation. It received FDA 510(k) clearance on 2006-09-01 under 510(k) number K062223. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGFA MODEL CR30-X?

AGFA MODEL CR30-X is a medical device that received FDA 510(k) clearance on 2006-09-01. The listed applicant is Agfa Corporation. The 510(k) number is K062223.

When did AGFA MODEL CR30-X receive FDA 510(k) clearance?

AGFA MODEL CR30-X received FDA 510(k) clearance on 2006-09-01, under 510(k) number K062223.

Who is the listed applicant for AGFA MODEL CR30-X?

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

What is the FDA product code for AGFA MODEL CR30-X?

The FDA product code for AGFA MODEL CR30-X is MQB.

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Other records listing Agfa Corporation 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.

K062742CR 85-XK053634COMPUTED RADIOGRAPHY SYSTEM WITH NX 1.0 WORKSTATIONK052251DRYSTAR MODEL 5500

Related Devices (Code: MQB)

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

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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