Argyle Sentinel Seal Autotransfusion System

FDA 510(k) K864374 · Sherwood Medical Co.

Substantially Equivalent

510(k) numberK864374

Submission

Device name
Argyle Sentinel Seal Autotransfusion System
Applicant
Sherwood Medical Co.
St. Louis, MO, US
Received
November 5, 1986
Decision date
March 16, 1987
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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Questions and answers

When was Argyle Sentinel Seal Autotransfusion System cleared by the FDA?

Argyle Sentinel Seal Autotransfusion System (K864374) received a 510(k) decision of Substantially Equivalent on March 16, 1987, 131 days after the submission was received.

What is the product code of K864374?

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