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SERIES 7000/HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K851971
510(k) Type
Traditional
Applicant
PFIZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1985
Days to Decision
44 days

SERIES 7000/HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K851971
510(k) Type
Traditional
Applicant
PFIZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1985
Days to Decision
44 days