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SPECTRA305

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820492
510(k) Type
Traditional
Applicant
ULTRALITE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1982
Days to Decision
36 days

SPECTRA305

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820492
510(k) Type
Traditional
Applicant
ULTRALITE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1982
Days to Decision
36 days