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ANALYZER, IMPACT 200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790072
510(k) Type
Traditional
Applicant
GILFORD INSTRUMENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1979
Days to Decision
42 days

ANALYZER, IMPACT 200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790072
510(k) Type
Traditional
Applicant
GILFORD INSTRUMENT LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1979
Days to Decision
42 days