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FDA 510(k)

CHASE BLOOD VESSEL SHUNT

K-Number: K972665 · 1997-08-22

ApplicantChase Medical, Inc.
Decision Date1997-08-22
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHASE BLOOD VESSEL SHUNT is the device name listed in this FDA 510(k) record. The listed applicant is Chase Medical, Inc.. It received FDA 510(k) clearance on 1997-08-22 under 510(k) number K972665. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHASE BLOOD VESSEL SHUNT?

CHASE BLOOD VESSEL SHUNT is a medical device that received FDA 510(k) clearance on 1997-08-22. The listed applicant is Chase Medical, Inc.. The 510(k) number is K972665.

When did CHASE BLOOD VESSEL SHUNT receive FDA 510(k) clearance?

CHASE BLOOD VESSEL SHUNT received FDA 510(k) clearance on 1997-08-22, under 510(k) number K972665.

Who is the listed applicant for CHASE BLOOD VESSEL SHUNT?

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

What is the FDA product code for CHASE BLOOD VESSEL SHUNT?

The FDA product code for CHASE BLOOD VESSEL SHUNT is DWF.

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Other records listing Chase Medical, 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.

K032531CHASE CARDIAC ANALYSIS SYSTEMK022093CHASE CARDIOVASCULAR PATCH KITK021129CHARE CARIOVASCULAR PATCHK020233CHASE CARDIOVASCULAR PATCH KITK020132CHASE CARDIOVASCULAR PATCH KITK012248CHASE CARDIOVASCULAR PATCH

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Related Devices (Code: DWF)

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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