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NEUROPAC ULTRA II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781829
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1978
Days to Decision
23 days

NEUROPAC ULTRA II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781829
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1978
Days to Decision
23 days