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BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES

Page Type
Cleared 510(K)
510(k) Number
K020538
510(k) Type
Traditional
Applicant
BOEHRINGER LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2002
Days to Decision
85 days
Submission Type
Statement

BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES

Page Type
Cleared 510(K)
510(k) Number
K020538
510(k) Type
Traditional
Applicant
BOEHRINGER LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2002
Days to Decision
85 days
Submission Type
Statement