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FDA 510(k)

EXCEL MODEL 2110

K-Number: K910727 · 1992-01-17

ApplicantExcel Medical Systems, Inc.
Decision Date1992-01-17
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EXCEL MODEL 2110 is the device name listed in this FDA 510(k) record. The listed applicant is Excel Medical Systems, Inc.. It received FDA 510(k) clearance on 1992-01-17 under 510(k) number K910727. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXCEL MODEL 2110?

EXCEL MODEL 2110 is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Excel Medical Systems, Inc.. The 510(k) number is K910727.

When did EXCEL MODEL 2110 receive FDA 510(k) clearance?

EXCEL MODEL 2110 received FDA 510(k) clearance on 1992-01-17, under 510(k) number K910727.

Who is the listed applicant for EXCEL MODEL 2110?

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

What is the FDA product code for EXCEL MODEL 2110?

The FDA product code for EXCEL MODEL 2110 is GZJ.

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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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