510(k) K772282

HODGE TUBE by Mallinckrodt Critical Care — Product Code FEG

K772282 is an FDA 510(k) premarket notification submitted by Mallinckrodt Critical Care for the device "HODGE TUBE". The FDA issued a decision of Substantially Equivalent on March 9, 1978. The device falls under product code FEG (Tube, Double Lumen For Intestinal Decompression And/Or Intubation), a Class II device regulated under 21 CFR 876.5980. Mallinckrodt Critical Care has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 9, 1978
Date Received
December 12, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tube, Double Lumen For Intestinal Decompression And/Or Intubation
Device Class
Class II
Regulation Number
876.5980
Review Panel
GU
Submission Type