Surgical Vascular Clamp

FDA 510(k) K973080 · Walter Lorenz Surgical, Inc.

Substantially Equivalent

510(k) numberK973080

Submission

Device name
Surgical Vascular Clamp
Applicant
Walter Lorenz Surgical, Inc.
Jacksonville, FL, US
Received
August 18, 1997
Decision date
February 23, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DXC – Clamp, Vascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4450
Specialty
Cardiovascular

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Questions and answers

When was Surgical Vascular Clamp cleared by the FDA?

Surgical Vascular Clamp (K973080) received a 510(k) decision of Substantially Equivalent on February 23, 1998, 189 days after the submission was received.

What is the product code of K973080?

The FDA product code is DXC – Clamp, Vascular, a Class II (moderate risk) device regulated under 21 CFR 870.4450.