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FDA 510(k)

KONTRON VITALMON 5010 PATIENT MONITOR

K-Number: K852249 · 1986-10-16

ApplicantKontron Instruments, Inc.
Decision Date1986-10-16
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KONTRON VITALMON 5010 PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Kontron Instruments, Inc.. It received FDA 510(k) clearance on 1986-10-16 under 510(k) number K852249. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONTRON VITALMON 5010 PATIENT MONITOR?

KONTRON VITALMON 5010 PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1986-10-16. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K852249.

When did KONTRON VITALMON 5010 PATIENT MONITOR receive FDA 510(k) clearance?

KONTRON VITALMON 5010 PATIENT MONITOR received FDA 510(k) clearance on 1986-10-16, under 510(k) number K852249.

Who is the listed applicant for KONTRON VITALMON 5010 PATIENT MONITOR?

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

What is the FDA product code for KONTRON VITALMON 5010 PATIENT MONITOR?

The FDA product code for KONTRON VITALMON 5010 PATIENT MONITOR is BZQ.

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Other records listing Kontron Instruments, Inc. as applicant

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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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