Last synced on 24 March 2023 at 11:04 pm

SYLVAN PEDIASCAN 200 TRANSILLUMINATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901309
510(k) Type
Traditional
Applicant
SYLVAN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1990
Days to Decision
65 days

SYLVAN PEDIASCAN 200 TRANSILLUMINATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901309
510(k) Type
Traditional
Applicant
SYLVAN CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1990
Days to Decision
65 days