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FDA 510(k)

CLOSED CHEST SUPPORT CIRCUIT

K-Number: K893207 · 1989-12-12

Decision Date1989-12-12
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLOSED CHEST SUPPORT CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Blood Systems, Inc.. It received FDA 510(k) clearance on 1989-12-12 under 510(k) number K893207. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLOSED CHEST SUPPORT CIRCUIT?

CLOSED CHEST SUPPORT CIRCUIT is a medical device that received FDA 510(k) clearance on 1989-12-12. The listed applicant is Medtronic Blood Systems, Inc.. The 510(k) number is K893207.

When did CLOSED CHEST SUPPORT CIRCUIT receive FDA 510(k) clearance?

CLOSED CHEST SUPPORT CIRCUIT received FDA 510(k) clearance on 1989-12-12, under 510(k) number K893207.

Who is the listed applicant for CLOSED CHEST SUPPORT CIRCUIT?

The FDA 510(k) record lists Medtronic Blood Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLOSED CHEST SUPPORT CIRCUIT?

The FDA product code for CLOSED CHEST SUPPORT CIRCUIT is DTZ.

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 Medtronic Blood Systems, 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.

View all 15 devices →

Related Devices (Code: DTZ)

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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