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FDA 510(k)

MINIMON 7132B PATIENT MONITOR

K-Number: K882198 · 1988-07-28

ApplicantKontron Instruments, Inc.
Decision Date1988-07-28
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIMON 7132B 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 1988-07-28 under 510(k) number K882198. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIMON 7132B PATIENT MONITOR?

MINIMON 7132B PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K882198.

When did MINIMON 7132B PATIENT MONITOR receive FDA 510(k) clearance?

MINIMON 7132B PATIENT MONITOR received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882198.

Who is the listed applicant for MINIMON 7132B 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 MINIMON 7132B PATIENT MONITOR?

The FDA product code for MINIMON 7132B PATIENT MONITOR is DPS.

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Other records listing Kontron Instruments, Inc. as applicant

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Related Devices (Code: DPS)

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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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