Last synced on 2 May 2025 at 11:05 pm

KEELER PULSAIR 3000 NON CONTACT TONOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990257
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1999
Days to Decision
57 days
Submission Type
Statement

KEELER PULSAIR 3000 NON CONTACT TONOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990257
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1999
Days to Decision
57 days
Submission Type
Statement