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GLIDESHEATH SLENDER MODEL RM* ES6J10HQS, GLIDESHEATH SLENDER MODEL RM* ES6F16HQ, GLIDESHEATH SLENDER MODEL RM * RS6J10PQ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122980
510(k) Type
Traditional
Applicant
Terumo Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2012
Days to Decision
76 days
Submission Type
Summary

GLIDESHEATH SLENDER MODEL RM* ES6J10HQS, GLIDESHEATH SLENDER MODEL RM* ES6F16HQ, GLIDESHEATH SLENDER MODEL RM * RS6J10PQ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122980
510(k) Type
Traditional
Applicant
Terumo Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2012
Days to Decision
76 days
Submission Type
Summary