Last synced on 14 November 2025 at 11:06 pm

ESOPHAGEAL MOTILITY PROBE

Page Type
Cleared 510(K)
510(k) Number
K811083
510(k) Type
Traditional
Applicant
KONIGSBERG INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1981
Days to Decision
114 days

ESOPHAGEAL MOTILITY PROBE

Page Type
Cleared 510(K)
510(k) Number
K811083
510(k) Type
Traditional
Applicant
KONIGSBERG INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1981
Days to Decision
114 days