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FDA 510(k)

DATA EXCHANGE SYSTEM, MODEL 24

K-Number: K890921 · 1989-06-08

Decision Date1989-06-08
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DATA EXCHANGE SYSTEM, MODEL 24 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Life Support Systems. It received FDA 510(k) clearance on 1989-06-08 under 510(k) number K890921. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATA EXCHANGE SYSTEM, MODEL 24?

DATA EXCHANGE SYSTEM, MODEL 24 is a medical device that received FDA 510(k) clearance on 1989-06-08. The listed applicant is Siemens Life Support Systems. The 510(k) number is K890921.

When did DATA EXCHANGE SYSTEM, MODEL 24 receive FDA 510(k) clearance?

DATA EXCHANGE SYSTEM, MODEL 24 received FDA 510(k) clearance on 1989-06-08, under 510(k) number K890921.

Who is the listed applicant for DATA EXCHANGE SYSTEM, MODEL 24?

The FDA 510(k) record lists Siemens Life Support Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DATA EXCHANGE SYSTEM, MODEL 24?

The FDA product code for DATA EXCHANGE SYSTEM, MODEL 24 is CBK.

Related Clinical Trials

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.

Other records listing Siemens Life Support Systems 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.

Related Devices (Code: CBK)

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.

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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