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FDA 510(k)

AGILENT M2636B TELEMON B MONITOR (TELEMON B)

K-Number: K011824 · 2001-07-02

ApplicantAgilent Technologies, Inc.
Decision Date2001-07-02
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AGILENT M2636B TELEMON B MONITOR (TELEMON B) 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 2001-07-02 under 510(k) number K011824. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGILENT M2636B TELEMON B MONITOR (TELEMON B)?

AGILENT M2636B TELEMON B MONITOR (TELEMON B) is a medical device that received FDA 510(k) clearance on 2001-07-02. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K011824.

When did AGILENT M2636B TELEMON B MONITOR (TELEMON B) receive FDA 510(k) clearance?

AGILENT M2636B TELEMON B MONITOR (TELEMON B) received FDA 510(k) clearance on 2001-07-02, under 510(k) number K011824.

Who is the listed applicant for AGILENT M2636B TELEMON B MONITOR (TELEMON B)?

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 AGILENT M2636B TELEMON B MONITOR (TELEMON B)?

The FDA product code for AGILENT M2636B TELEMON B MONITOR (TELEMON B) is DSI.

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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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