Last synced on 14 November 2025 at 11:06 pm

GASTROINTESTINAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K870508
510(k) Type
Traditional
Applicant
PENN MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1987
Days to Decision
95 days

GASTROINTESTINAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K870508
510(k) Type
Traditional
Applicant
PENN MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1987
Days to Decision
95 days