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NICOLET NEUROPORT/ACE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883781
510(k) Type
Traditional
Applicant
NICOLET INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1989
Days to Decision
272 days

NICOLET NEUROPORT/ACE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883781
510(k) Type
Traditional
Applicant
NICOLET INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1989
Days to Decision
272 days