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FDA 510(k)

CP 100/30

K-Number: K953292 · 1995-11-22

Decision Date1995-11-22
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CP 100/30 is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Focus Imaging., Inc.. It received FDA 510(k) clearance on 1995-11-22 under 510(k) number K953292. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CP 100/30?

CP 100/30 is a medical device that received FDA 510(k) clearance on 1995-11-22. The listed applicant is Micro-Focus Imaging., Inc.. The 510(k) number is K953292.

When did CP 100/30 receive FDA 510(k) clearance?

CP 100/30 received FDA 510(k) clearance on 1995-11-22, under 510(k) number K953292.

Who is the listed applicant for CP 100/30?

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

What is the FDA product code for CP 100/30?

The FDA product code for CP 100/30 is IZL.

Other records listing Micro-Focus Imaging., 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.

Related Devices (Code: IZL)

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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