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FDA 510(k)

M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1

K-Number: K001711 · 2000-06-20

ApplicantAgilent Technologies, Inc.
Decision Date2000-06-20
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1 is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 2000-06-20 under 510(k) number K001711. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1?

M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1 is a medical device that received FDA 510(k) clearance on 2000-06-20. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K001711.

When did M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1 receive FDA 510(k) clearance?

M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1 received FDA 510(k) clearance on 2000-06-20, under 510(k) number K001711.

Who is the listed applicant for M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1?

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

What is the FDA product code for M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1?

The FDA product code for M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1 is IYN.

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Related Devices (Code: IYN)

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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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