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LED.L, LED.M, LED.G, LED.B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080025
510(k) Type
Traditional
Applicant
GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2008
Days to Decision
75 days
Submission Type
Statement

LED.L, LED.M, LED.G, LED.B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080025
510(k) Type
Traditional
Applicant
GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2008
Days to Decision
75 days
Submission Type
Statement