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MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980980
510(k) Type
Traditional
Applicant
KONIGSBERG INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1998
Days to Decision
90 days
Submission Type
Statement

MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980980
510(k) Type
Traditional
Applicant
KONIGSBERG INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1998
Days to Decision
90 days
Submission Type
Statement