Venapulse Models VP-25 and VP-50

FDA 510(k) K903894 · Aci Medical, Inc.

Substantially Equivalent

510(k) numberK903894

Submission

Device name
Venapulse Models VP-25 and VP-50
Applicant
Aci Medical, Inc.
Sun Valley, CA, US
Received
August 23, 1990
Decision date
April 3, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JOW – Sleeve, Limb, Compressible
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5800
Specialty
Cardiovascular

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K903532Unna-Sleeve(Tm)LLK · Traditional 11/02/1990SE
K881291Air Plethysmograph Model APG-1000DSB · Traditional 10/14/1988SE
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Questions and answers

When was Venapulse Models VP-25 and VP-50 cleared by the FDA?

Venapulse Models VP-25 and VP-50 (K903894) received a 510(k) decision of Substantially Equivalent on April 3, 1991, 223 days after the submission was received.

What is the product code of K903894?

The FDA product code is JOW – Sleeve, Limb, Compressible, a Class II (moderate risk) device regulated under 21 CFR 870.5800.