Gimmi GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K092421ALPHAHYSTEROSCOPE, FIBEROPTIC, OPERATIVE AND DIAGNOSTICFebruary 12, 2010
K093125ALPHAXENON LIGHT 180 W AND 300 WJanuary 27, 2010
K081640GIMMI ANEURYSM CLIPS AND APPLYING FORCEPSMay 6, 2009
K012869GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX, ZXXX.XX,S.XXXX.XX, K0142.25March 11, 2002
K012660GIMMI'ALPHA' ENDOSCOPES & ACCESSORIESDecember 20, 2001
K013731GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # November 27, 2001