Gimmi GmbH
Gimmi GmbH appears in FDA public data with 0 recalls, 6 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 12, 2010.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K092421 | ALPHAHYSTEROSCOPE, FIBEROPTIC, OPERATIVE AND DIAGNOSTIC | February 12, 2010 |
| K093125 | ALPHAXENON LIGHT 180 W AND 300 W | January 27, 2010 |
| K081640 | GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS | May 6, 2009 |
| K012869 | GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX, ZXXX.XX,S.XXXX.XX, K0142.25 | March 11, 2002 |
| K012660 | GIMMI'ALPHA' ENDOSCOPES & ACCESSORIES | December 20, 2001 |
| K013731 | GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # | November 27, 2001 |