Spsmedical Sporview Pa Culture Set

FDA 510(k) K043135 · Spsmedical Supply Corp.

Substantially Equivalent

510(k) numberK043135

Submission

Device name
Spsmedical Sporview Pa Culture Set
Applicant
Spsmedical Supply Corp.
Rush, NY, US
Received
November 12, 2004
Decision date
January 13, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MRB – Indicator, Biological, Liquid Chemical Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

Other 510(k)s with product code MRB

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K081879Spsmedical Sporview Pa Culture SetMRB · Special Spsmedical Supply Corp.07/30/2008SE
K053212Raven PropactMRB · Special Raven Biological Laboratories, Inc.02/15/2006SE
K031114Pro-Pact Peracetic Acid Culture Test Kit, Model C-3PAMRB · Traditional Raven Biological Laboratories, Inc.03/03/2004SE

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K102363Spsmedical Emplus 270 F Steam Emulator Model EMP-104, EMP-1004JOJ · Traditional 01/27/2011SE
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K081879Spsmedical Sporview Pa Culture SetMRB · Special 07/30/2008SE
K070595Sporview Steam Self-Contained Biological IndicatorFRC · Traditional 05/24/2007SE
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K051173Spsmedical Sporview Plus Steam Bi Test PackFRC · Special 05/27/2005SE

Questions and answers

When was Spsmedical Sporview Pa Culture Set cleared by the FDA?

Spsmedical Sporview Pa Culture Set (K043135) received a 510(k) decision of Substantially Equivalent on January 13, 2005, 62 days after the submission was received.

What is the product code of K043135?

The FDA product code is MRB – Indicator, Biological, Liquid Chemical Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.