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AMBULATORY (HOLTER) RECORDING, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K922027
510(k) Type
Traditional
Applicant
BIOSENSOR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1993
Days to Decision
328 days
Submission Type
Statement

AMBULATORY (HOLTER) RECORDING, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K922027
510(k) Type
Traditional
Applicant
BIOSENSOR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1993
Days to Decision
328 days
Submission Type
Statement