Last synced on 4 February 2023 at 10:33 pm

KEELER MULTILASE 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942180
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1994
Days to Decision
202 days
Submission Type
Statement

KEELER MULTILASE 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942180
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1994
Days to Decision
202 days
Submission Type
Statement