CENTURION CIRCLAMP
K-Number: K890897 · 1989-03-28
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Device Summary
Frequently Asked Questions
What is the CENTURION CIRCLAMP?
CENTURION CIRCLAMP is a medical device that received FDA 510(k) clearance on 1989-03-28. The listed applicant is Tri-State Hospital Supply Corp.. The 510(k) number is K890897.
When did CENTURION CIRCLAMP receive FDA 510(k) clearance?
CENTURION CIRCLAMP received FDA 510(k) clearance on 1989-03-28, under 510(k) number K890897.
Who is the listed applicant for CENTURION CIRCLAMP?
The FDA 510(k) record lists Tri-State Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTURION CIRCLAMP?
The FDA product code for CENTURION CIRCLAMP is HFX.
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 Tri-State Hospital Supply 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.
Related Devices (Code: HFX)
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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