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PROBE(TM) MODELS 700 AND 1000

Page Type
Cleared 510(K)
510(k) Number
K883749
510(k) Type
Traditional
Applicant
PACKARD INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1988
Days to Decision
70 days

PROBE(TM) MODELS 700 AND 1000

Page Type
Cleared 510(K)
510(k) Number
K883749
510(k) Type
Traditional
Applicant
PACKARD INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1988
Days to Decision
70 days