Sirocco Thermal Regulating System

FDA 510(k) K102856 · Galmaz Biotech S.L.

Substantially Equivalent

510(k) numberK102856

Submission

Device name
Sirocco Thermal Regulating System
Applicant
Galmaz Biotech S.L.
Hudson, WI, US
Received
September 29, 2010
Decision date
June 30, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
DWJ – System, Thermal Regulating
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5900
Specialty
Cardiovascular

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was Sirocco Thermal Regulating System cleared by the FDA?

Sirocco Thermal Regulating System (K102856) received a 510(k) decision of Substantially Equivalent on June 30, 2011, 274 days after the submission was received.

What is the product code of K102856?

The FDA product code is DWJ – System, Thermal Regulating, a Class II (moderate risk) device regulated under 21 CFR 870.5900.