Last synced on 27 January 2023 at 11:04 pm

BRILLETTE MODEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842835
510(k) Type
Traditional
Applicant
CILLUS COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1984
Days to Decision
124 days

BRILLETTE MODEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842835
510(k) Type
Traditional
Applicant
CILLUS COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1984
Days to Decision
124 days