Amerimed US Corp.

FDA Regulatory Profile

Amerimed US Corp. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 14, 1989.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K891722LATEX EXAM GLOVES (MFG. SHANGHAI MEHECO)July 14, 1989
K891437PATIENT EXAMINATION GLOVES (LATEX)May 31, 1989
K891436PATIENT EXAMINATION GLOVES (LATEX)May 31, 1989
K890967VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)May 4, 1989
K883522AMERIMED ULTRASONIC SURGICAL ASPIRATION KITSeptember 30, 1988