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FDA 510(k)

XCALIBER

K-Number: K904818 · 1990-11-07

ApplicantEverest & Jennings, Inc.
Decision Date1990-11-07
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

XCALIBER is the device name listed in this FDA 510(k) record. The listed applicant is Everest & Jennings, Inc.. It received FDA 510(k) clearance on 1990-11-07 under 510(k) number K904818. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XCALIBER?

XCALIBER is a medical device that received FDA 510(k) clearance on 1990-11-07. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K904818.

When did XCALIBER receive FDA 510(k) clearance?

XCALIBER received FDA 510(k) clearance on 1990-11-07, under 510(k) number K904818.

Who is the listed applicant for XCALIBER?

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

What is the FDA product code for XCALIBER?

The FDA product code for XCALIBER is ITI.

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Other records listing Everest & Jennings, Inc. as applicant

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Related Devices (Code: ITI)

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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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