FDA 510(k)

MPR-814

K-Number: K940442 · 1994-06-09

Decision Date1994-06-09

Product CodeIYB

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MPR-814 is the device name listed in this FDA 510(k) record. The listed applicant is Xri, Inc.. It received FDA 510(k) clearance on 1994-06-09 under 510(k) number K940442. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPR-814?

MPR-814 is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Xri, Inc.. The 510(k) number is K940442.

When did MPR-814 receive FDA 510(k) clearance?

MPR-814 received FDA 510(k) clearance on 1994-06-09, under 510(k) number K940442.

Who is the listed applicant for MPR-814?

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

What is the FDA product code for MPR-814?

The FDA product code for MPR-814 is IYB.

Related Devices (Code: IYB)

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.

K935123SUPERSTAND 300Wuestec Medical, Inc.K946261MTS-007, STS-008, SSMTS-010, EURO-40, 72, SUPER EURO 4072, 5000Scott Imaging Intl., Inc.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K935004MODEL ALPHA TS-2Dpa Consulting, Inc.K933253SUPERSTAND 3000Wuestec Medical, Inc.

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.