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NEUROPAC ULTRA II

Page Type
Cleared 510(K)
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)
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