Last synced on 25 November 2022 at 11:04 pm

SINGLE USE ELECTROSURGICAL KNIFE SERIES, MODEL KD-610L, KD-611L, KD-620LR, KD-630L, KF-640L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092309
510(k) Type
Traditional
Applicant
OLYMPUS MEDICAL SYSTEMS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2009
Days to Decision
92 days
Submission Type
Summary

SINGLE USE ELECTROSURGICAL KNIFE SERIES, MODEL KD-610L, KD-611L, KD-620LR, KD-630L, KF-640L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092309
510(k) Type
Traditional
Applicant
OLYMPUS MEDICAL SYSTEMS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2009
Days to Decision
92 days
Submission Type
Summary