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BETA I & BETA II

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K811082
510(k) Type
Traditional
Applicant
PORTA RAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1981
Days to Decision
30 days

BETA I & BETA II

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K811082
510(k) Type
Traditional
Applicant
PORTA RAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1981
Days to Decision
30 days