Surgactivator

FDA 510(k) K951569 · Deschutes Medical Products, Inc.

Substantially Equivalent

510(k) numberK951569

Submission

Device name
Surgactivator
Applicant
Deschutes Medical Products, Inc.
Bend, OR, US
Received
April 4, 1995
Decision date
June 6, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LJH – System, Irrigation, Urological
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

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Questions and answers

When was Surgactivator cleared by the FDA?

Surgactivator (K951569) received a 510(k) decision of Substantially Equivalent on June 6, 1995, 63 days after the submission was received.

What is the product code of K951569?

The FDA product code is LJH – System, Irrigation, Urological, a Class II (moderate risk) device regulated under 21 CFR 876.5130.