Gimmi GmbH
Gimmi GmbH holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2026.
Top product codes for Gimmi GmbH
Recent clearances by Gimmi GmbH
- K261179 — AlphaTriPart - Monopolar MIC Instruments
- K092421 — ALPHAHYSTEROSCOPE, FIBEROPTIC, OPERATIVE AND DIAGNOSTIC
- K093125 — ALPHAXENON LIGHT 180 W AND 300 W
- K081640 — GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS
- K012869 — GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX, ZXXX.XX,S.XXXX.XX, K0142.25
- K012660 — GIMMI'ALPHA' ENDOSCOPES & ACCESSORIES
- K013731 — GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # E.8189.00/01/02/03
Data sourced from openFDA. This site is unofficial and independent of the FDA.