Last synced on 4 February 2023 at 10:33 pm

MODIFIED NICOLET VIKING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880573
510(k) Type
Traditional
Applicant
NICOLET BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
41 days

MODIFIED NICOLET VIKING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880573
510(k) Type
Traditional
Applicant
NICOLET BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
41 days