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TONOPACH ULTRASONIC TONOMETER/PACHYMETER MODEL P-201 (THE TONOPACH)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042099
510(k) Type
Traditional
Applicant
RETINAPHARMA TECHNOLOGIES INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
128 days
Submission Type
Summary

TONOPACH ULTRASONIC TONOMETER/PACHYMETER MODEL P-201 (THE TONOPACH)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042099
510(k) Type
Traditional
Applicant
RETINAPHARMA TECHNOLOGIES INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
128 days
Submission Type
Summary