Last synced on 25 November 2022 at 11:04 pm

PLASIATEK ACTUATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041917
510(k) Type
Traditional
Applicant
PLASIATEK, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2005
Days to Decision
175 days
Submission Type
Summary

PLASIATEK ACTUATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041917
510(k) Type
Traditional
Applicant
PLASIATEK, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2005
Days to Decision
175 days
Submission Type
Summary