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FDA 510(k)

COAGULATION CONTROL CONTAINING HEMOGLOBIN

K-Number: K925340 · 1993-03-23

ApplicantAnalytical Control Systems, Inc.
Decision Date1993-03-23
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

COAGULATION CONTROL CONTAINING HEMOGLOBIN is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Control Systems, Inc.. It received FDA 510(k) clearance on 1993-03-23 under 510(k) number K925340. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAGULATION CONTROL CONTAINING HEMOGLOBIN?

COAGULATION CONTROL CONTAINING HEMOGLOBIN is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is Analytical Control Systems, Inc.. The 510(k) number is K925340.

When did COAGULATION CONTROL CONTAINING HEMOGLOBIN receive FDA 510(k) clearance?

COAGULATION CONTROL CONTAINING HEMOGLOBIN received FDA 510(k) clearance on 1993-03-23, under 510(k) number K925340.

Who is the listed applicant for COAGULATION CONTROL CONTAINING HEMOGLOBIN?

The FDA 510(k) record lists Analytical Control Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAGULATION CONTROL CONTAINING HEMOGLOBIN?

The FDA product code for COAGULATION CONTROL CONTAINING HEMOGLOBIN is JPA.

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Other records listing Analytical Control Systems, Inc. as applicant

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Related Devices (Code: JPA)

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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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