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LIFE-TECH #5102 VISULAB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812180
510(k) Type
Traditional
Applicant
LIFE-TECH INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1981
Days to Decision
18 days

LIFE-TECH #5102 VISULAB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812180
510(k) Type
Traditional
Applicant
LIFE-TECH INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1981
Days to Decision
18 days