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FDA 510(k)

Universal 1417PI

K-Number: K252996 · 2026-06-12

ApplicantKonica Minolta Healthcare Americas, Inc.
Decision Date2026-06-12
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Universal 1417PI is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta Healthcare Americas, Inc.. It received FDA 510(k) clearance on 2026-06-12 under 510(k) number K252996. 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 Universal 1417PI?

Universal 1417PI is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Konica Minolta Healthcare Americas, Inc.. The 510(k) number is K252996.

When did Universal 1417PI receive FDA 510(k) clearance?

Universal 1417PI received FDA 510(k) clearance on 2026-06-12, under 510(k) number K252996.

Who is the listed applicant for Universal 1417PI?

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

What is the FDA product code for Universal 1417PI?

The FDA product code for Universal 1417PI is MQB.

Other records listing Konica Minolta Healthcare Americas, Inc. as applicant

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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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