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PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900314
510(k) Type
Traditional
Applicant
PERCUSSIONAIRE CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/26/1990
Days to Decision
277 days

PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900314
510(k) Type
Traditional
Applicant
PERCUSSIONAIRE CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/26/1990
Days to Decision
277 days