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Data / Medical devices / Spain / Hersill, S.L.

Hersill, S.L.: FDA-registered device maker in MOSTOLES (MADRID) Madrid(Province), Spain, 1 510(k) clearance

Hersill, S.L. is registered with the FDA (registration 3007360714) in MOSTOLES (MADRID) Madrid(Province), Spain. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 27, 2010. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3007360714
Address
C/ Puerto De Navacerrada, 3, MOSTOLES (MADRID) Madrid(Province), Spain, 28935
Owner or operator
HERSILL, S.L. (10027484)
Roles
Manufacturer
First device listed
November 12, 2008
Registered through
2026
Brand names listed
COLLECTION JARS, Care-e-vac C/I, Care-e-vac EMS, Care-e-vac Plus, FLOW SELECTOR, HERSILL FLOWMETERS, HUMIDIFIER, OXYLL and more

Devices it lists

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
April 27, 2010K093241V7 PORTABLE SUCTION UNITSBTASubstantially EquivalentHersill, S.L.accessdata.fda.gov

Compare with other makers

Updated April 27, 2010. 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.