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Data / Medical devices / United States / Revolutionary Science

Revolutionary Science: FDA-registered device maker in Shafer, MN, United States, 2 510(k) clearances

Revolutionary Science is registered with the FDA (registration 3009519707) in Shafer, MN, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 23, 2013. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3009519707
Address
17319 Lake Blvd, Shafer, MN, United States, 55074
Owner or operator
Revolutionary Science (10040300)
Roles
Manufacturer
First device listed
March 29, 2012
Registered through
2026
Brand names listed
RS-SC-102; SaniClave 102, RS-SC-200; RS-SC-200P; RS-SC-200M; RS-SC-250; SaniClave 200; SaniClave 200P; SaniClave 200M; SaniClave 250

Devices it lists

DeviceProduct codeClassRoleSource
Sterilizer, SteamFLE2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 23, 2013K122978SANICLAVE 102, MODEL RS-SC-102FLESubstantially EquivalentAlternative Pioneering Research and Developmentaccessdata.fda.gov
January 11, 2012K112811SANICLAVE 200FLESubstantially EquivalentAlternative Pioneering Research and Developmentaccessdata.fda.gov

Compare with other makers

Updated May 23, 2013. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.