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VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K905235
510(k) Type
Traditional
Applicant
PERCUSSIONAIRE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1991
Days to Decision
177 days

VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K905235
510(k) Type
Traditional
Applicant
PERCUSSIONAIRE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1991
Days to Decision
177 days