Last synced on 14 November 2025 at 11:06 pm

MODIFIED NICOLET VIKING SYSTEM

Page Type
Cleared 510(K)
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)
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