Ronvig Instruments, Ltd.

FDA Regulatory Profile

Ronvig Instruments, Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 13, 2000.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002168ASPIJECT SELF-ASPIRATING DENTAL INJECTION SYRINGEOctober 13, 2000
K904279PAROJECT ANESTHETIC SYRINGEDecember 7, 1990