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FDA 510(k)

KONTRON KOLORMON 7250 PATIENT MONITOR

K-Number: K896417 · 1989-12-12

ApplicantKontron Instruments, Inc.
Decision Date1989-12-12
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KONTRON KOLORMON 7250 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 1989-12-12 under 510(k) number K896417. 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 KONTRON KOLORMON 7250 PATIENT MONITOR?

KONTRON KOLORMON 7250 PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1989-12-12. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K896417.

When did KONTRON KOLORMON 7250 PATIENT MONITOR receive FDA 510(k) clearance?

KONTRON KOLORMON 7250 PATIENT MONITOR received FDA 510(k) clearance on 1989-12-12, under 510(k) number K896417.

Who is the listed applicant for KONTRON KOLORMON 7250 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 KOLORMON 7250 PATIENT MONITOR?

The FDA product code for KONTRON KOLORMON 7250 PATIENT MONITOR is DPS.

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Other records listing Kontron Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K932268MODIFICATIONS TO INTRA-AORTIC BALLOONSK925248MODIFICATION OF INTRA-AORTIC BALLOON CATHETERSK923603INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATIONK905313KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT IIK9033449.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)K896437KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEM

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Related Devices (Code: DPS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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