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Reed Products, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K841898
FIRST RESPONSE EMERG. MEDICSL - BURNS
August 14, 1984
K841900
FIRST RESPONSE EMERG. EYE INJURIES
July 23, 1984
K841899
FIRST RESPONSE EMERG. MEDICAL SYS BONES
July 23, 1984
K841897
FIRST RESPONSE EMERG. MEDICAL SYSTEM
July 23, 1984