ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC
K-Number: K022480 · 2002-08-22
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Device Summary
Frequently Asked Questions
What is the ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC?
ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC is a medical device that received FDA 510(k) clearance on 2002-08-22. The listed applicant is Acmi Corporation. The 510(k) number is K022480.
When did ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC receive FDA 510(k) clearance?
ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC received FDA 510(k) clearance on 2002-08-22, under 510(k) number K022480.
Who is the listed applicant for ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC?
The FDA 510(k) record lists Acmi Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC?
The FDA product code for ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC is HIH.
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 Acmi Corporation 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: HIH)
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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