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FDA 510(k)

ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC

K-Number: K022480 · 2002-08-22

Decision Date2002-08-22
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC is the device name listed in this FDA 510(k) record. The listed applicant is Acmi Corporation. It received FDA 510(k) clearance on 2002-08-22 under 510(k) number K022480. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 16 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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