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RAYMAX 2100 MODELS 2130 & 2136

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883431
510(k) Type
Traditional
Applicant
RAYMAX MEDICAL CORP.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/12/1988
Days to Decision
28 days

RAYMAX 2100 MODELS 2130 & 2136

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883431
510(k) Type
Traditional
Applicant
RAYMAX MEDICAL CORP.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/12/1988
Days to Decision
28 days