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PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082786
510(k) Type
Traditional
Applicant
PEAK SURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2008
Days to Decision
71 days
Submission Type
Summary

PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082786
510(k) Type
Traditional
Applicant
PEAK SURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2008
Days to Decision
71 days
Submission Type
Summary