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FDA 510(k)

MINIMON 7136B PATIENT MONITOR

K-Number: K883109 · 1989-01-17

ApplicantKontron, Inc.
Decision Date1989-01-17
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIMON 7136B PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Kontron, Inc.. It received FDA 510(k) clearance on 1989-01-17 under 510(k) number K883109. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIMON 7136B PATIENT MONITOR?

MINIMON 7136B PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Kontron, Inc.. The 510(k) number is K883109.

When did MINIMON 7136B PATIENT MONITOR receive FDA 510(k) clearance?

MINIMON 7136B PATIENT MONITOR received FDA 510(k) clearance on 1989-01-17, under 510(k) number K883109.

Who is the listed applicant for MINIMON 7136B PATIENT MONITOR?

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

What is the FDA product code for MINIMON 7136B PATIENT MONITOR?

The FDA product code for MINIMON 7136B PATIENT MONITOR is DRT.

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Related Devices (Code: DRT)

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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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