Last synced on 30 September 2022 at 11:05 pm

STORZ PHACOEMULSIFICATION NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K946176
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1995
Days to Decision
57 days
Submission Type
Summary

STORZ PHACOEMULSIFICATION NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K946176
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1995
Days to Decision
57 days
Submission Type
Summary