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AUTOLYZER 801 SYSTEM (AUTOMATED CELL COUNTER)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875346
510(k) Type
Traditional
Applicant
CONTRAVES MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1988
Days to Decision
98 days

AUTOLYZER 801 SYSTEM (AUTOMATED CELL COUNTER)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875346
510(k) Type
Traditional
Applicant
CONTRAVES MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1988
Days to Decision
98 days