60 Micro Volume Extension Set W/.22 Micron Filter, 21 Extension Set W/1.2 Mivton Gilyrt, Inj. Site, Clamp

FDA 510(k) K952663 · Distronic Sterile Products, Inc.

Substantially Equivalent

510(k) numberK952663

Submission

Device name
60 Micro Volume Extension Set W/.22 Micron Filter, 21 Extension Set W/1.2 Mivton Gilyrt, Inj. Site, Clamp
Applicant
Distronic Sterile Products, Inc.
Portsmouth, NH, US
Received
June 12, 1995
Decision date
July 14, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPK – Tubing, Fluid Delivery
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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More from Sysmex Corp.

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K954984Minibore Stopcock SetFMG · Traditional 01/23/1996SE
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K952664Solution Administration SetFPA · Traditional 08/07/1995SE
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Questions and answers

When was 60 Micro Volume Extension Set W/.22 Micron Filter, 21 Extension Set W/1.2 Mivton Gilyrt, Inj. Site, Clamp cleared by the FDA?

60 Micro Volume Extension Set W/.22 Micron Filter, 21 Extension Set W/1.2 Mivton Gilyrt, Inj. Site, Clamp (K952663) received a 510(k) decision of Substantially Equivalent on July 14, 1995, 32 days after the submission was received.

What is the product code of K952663?

The FDA product code is FPK – Tubing, Fluid Delivery, a Class II (moderate risk) device regulated under 21 CFR 880.5440.