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FDA 510(k)

CHASE VESSEL OCCLUDER

K-Number: K964390 · 1997-01-31

ApplicantChase Medical, Inc.
Decision Date1997-01-31
Product CodeMJN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHASE VESSEL OCCLUDER 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 1997-01-31 under 510(k) number K964390. The device is classified under product code MJN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHASE VESSEL OCCLUDER?

CHASE VESSEL OCCLUDER is a medical device that received FDA 510(k) clearance on 1997-01-31. The listed applicant is Chase Medical, Inc.. The 510(k) number is K964390.

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

CHASE VESSEL OCCLUDER received FDA 510(k) clearance on 1997-01-31, under 510(k) number K964390.

Who is the listed applicant for CHASE VESSEL OCCLUDER?

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 VESSEL OCCLUDER?

The FDA product code for CHASE VESSEL OCCLUDER is MJN.

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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: MJN)

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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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