Sterile Soft-Temp

FDA 510(k) K962983 · Adroit Medical Systems, Inc.

Substantially Equivalent

510(k) numberK962983

Submission

Device name
Sterile Soft-Temp
Applicant
Adroit Medical Systems, Inc.
Loudon, TN, US
Received
August 1, 1996
Decision date
January 10, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ILO – Pack, Hot Or Cold, Water Circulating
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5720
Specialty
Physical Medicine

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More from Ormed GmbH

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K073712Soft Air, Model SA 4000 and Mistral Air, Model MA0100DWJ · Traditional 06/06/2008SE
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K970197HTP-1500 Localized Heat Therapy PumpILO · Traditional 09/10/1997SE
K921920Soft-TempDWJ · Traditional 12/11/1992SE
K921928Soft-CoverFMW · Traditional 11/06/1992SE

Questions and answers

When was Sterile Soft-Temp cleared by the FDA?

Sterile Soft-Temp (K962983) received a 510(k) decision of Substantially Equivalent on January 10, 1997, 162 days after the submission was received.

What is the product code of K962983?

The FDA product code is ILO – Pack, Hot Or Cold, Water Circulating, a Class II (moderate risk) device regulated under 21 CFR 890.5720.