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MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884782
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1989
Days to Decision
94 days

MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884782
510(k) Type
Traditional
Applicant
DYNATECH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/1989
Days to Decision
94 days