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FDA 510(k)

SYSTEM 90 AND SYSTEM 90T

K-Number: K913847 · 1992-03-11

Decision Date1992-03-11
Product CodeDSP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SYSTEM 90 AND SYSTEM 90T is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1992-03-11 under 510(k) number K913847. The device is classified under product code DSP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSTEM 90 AND SYSTEM 90T?

SYSTEM 90 AND SYSTEM 90T is a medical device that received FDA 510(k) clearance on 1992-03-11. The listed applicant is Datascope Corp.. The 510(k) number is K913847.

When did SYSTEM 90 AND SYSTEM 90T receive FDA 510(k) clearance?

SYSTEM 90 AND SYSTEM 90T received FDA 510(k) clearance on 1992-03-11, under 510(k) number K913847.

Who is the listed applicant for SYSTEM 90 AND SYSTEM 90T?

The FDA 510(k) record lists Datascope Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYSTEM 90 AND SYSTEM 90T?

The FDA product code for SYSTEM 90 AND SYSTEM 90T is DSP.

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 Datascope Corp. 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.

View all 135 devices →

Related Devices (Code: DSP)

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

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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