Last synced on 14 November 2025 at 11:06 pm

TYMPASNOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K953993
510(k) Type
Traditional
Applicant
HAMPTON PRECISION PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1995
Days to Decision
19 days
Submission Type
Summary

TYMPASNOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K953993
510(k) Type
Traditional
Applicant
HAMPTON PRECISION PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1995
Days to Decision
19 days
Submission Type
Summary