CHASE SUCKER
K-Number: K971022 · 1997-04-17
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Device Summary
Frequently Asked Questions
What is the CHASE SUCKER?
CHASE SUCKER is a medical device that received FDA 510(k) clearance on 1997-04-17. The listed applicant is Chase Medical, Inc.. The 510(k) number is K971022.
When did CHASE SUCKER receive FDA 510(k) clearance?
CHASE SUCKER received FDA 510(k) clearance on 1997-04-17, under 510(k) number K971022.
Who is the listed applicant for CHASE SUCKER?
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 SUCKER?
The FDA product code for CHASE SUCKER is GCX.
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 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.
Related Devices (Code: GCX)
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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