Zyno Medical Administration Set

FDA 510(k) K120685 · Zyno Medical, LLC

Substantially Equivalent

510(k) numberK120685

Submission

Device name
Zyno Medical Administration Set
Applicant
Zyno Medical, LLC
Natick, MA, US
Received
March 6, 2012
Decision date
September 7, 2012
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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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More from B.Braun Medical, Inc.

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Questions and answers

When was Zyno Medical Administration Set cleared by the FDA?

Zyno Medical Administration Set (K120685) received a 510(k) decision of Substantially Equivalent on September 7, 2012, 185 days after the submission was received.

What is the product code of K120685?

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