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ROBERTSON OBTURATION MONITOR INSUFFLA

Page Type
Cleared 510(K)
510(k) Number
K802374
510(k) Type
Traditional
Applicant
ENDOTEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1980
Days to Decision
56 days

ROBERTSON OBTURATION MONITOR INSUFFLA

Page Type
Cleared 510(K)
510(k) Number
K802374
510(k) Type
Traditional
Applicant
ENDOTEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1980
Days to Decision
56 days