Acu-Med Red Miser Hemothorax Blood Coll.

FDA 510(k) K791891 · Acumed Instruments Corp.

Substantially Equivalent

510(k) numberK791891

Submission

Device name
Acu-Med Red Miser Hemothorax Blood Coll.
Applicant
Acumed Instruments Corp.
Mchenry, IL, US
Received
September 25, 1979
Decision date
December 5, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAC – Apparatus, Autotransfusion
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5830
Specialty
Anesthesiology
Life-sustaining
Yes

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K791399Acu-Alert · Traditional 10/11/1979SE
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Questions and answers

When was Acu-Med Red Miser Hemothorax Blood Coll. cleared by the FDA?

Acu-Med Red Miser Hemothorax Blood Coll. (K791891) received a 510(k) decision of Substantially Equivalent on December 5, 1979, 71 days after the submission was received.

What is the product code of K791891?

The FDA product code is CAC – Apparatus, Autotransfusion, a Class II (moderate risk) device regulated under 21 CFR 868.5830.