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WEINGART MODEL 1000 SUNLAMP PRODUCT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863518
510(k) Type
Traditional
Applicant
WEINGART, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1986
Days to Decision
23 days

WEINGART MODEL 1000 SUNLAMP PRODUCT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863518
510(k) Type
Traditional
Applicant
WEINGART, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1986
Days to Decision
23 days