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Vomed Volzer Medizintechnik GmbH & Co.

FDA Regulatory Profile

Vomed Volzer Medizintechnik GmbH & Co. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 10, 2002.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023019VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000December 10, 2002
K022257VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 XXX & 9006 XXX-9011 XXXOctober 4, 2002
K022318VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIESSeptember 19, 2002

FDA data resources