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FDA 510(k)

KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM

K-Number: K870816 · 1988-03-01

ApplicantKontron Instruments, Inc.
Decision Date1988-03-01
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM 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 1988-03-01 under 510(k) number K870816. 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 KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM?

KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-01. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K870816.

When did KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM receive FDA 510(k) clearance?

KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM received FDA 510(k) clearance on 1988-03-01, under 510(k) number K870816.

Who is the listed applicant for KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM?

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 STRESSDATA STRESS DATA MANAGEMENT SYSTEM?

The FDA product code for KONTRON STRESSDATA STRESS DATA MANAGEMENT SYSTEM is DSI.

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Other records listing Kontron Instruments, Inc. as applicant

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Related Devices (Code: DSI)

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.

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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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