Last synced on 23 September 2022 at 11:05 pm

STELLAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002463
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2000
Days to Decision
90 days
Submission Type
Statement

STELLAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002463
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2000
Days to Decision
90 days
Submission Type
Statement