Cadd High-Volume Administration Sets with Flowstop

FDA 510(k) K031361 · Deltec, Inc.

Substantially Equivalent

510(k) numberK031361

Submission

Device name
Cadd High-Volume Administration Sets with Flowstop
Applicant
Deltec, Inc.
St. Paul, MN, US
Received
April 30, 2003
Decision date
May 23, 2003
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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Questions and answers

When was Cadd High-Volume Administration Sets with Flowstop cleared by the FDA?

Cadd High-Volume Administration Sets with Flowstop (K031361) received a 510(k) decision of Substantially Equivalent on May 23, 2003, 23 days after the submission was received.

What is the product code of K031361?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.