Atlas FDA

HODGE TUBE

FDA 510(k) clearance K772282 · decided 1978-03-09

Clearance details

K-number
K772282
Device name
HODGE TUBE
Applicant
Mallinckrodt Critical Care
Decision
Substantially Equivalent
Date received
1977-12-12
Decision date
1978-03-09
Days to decision
87 days
Clearance type
Traditional
Product code
FEG
Device class
2
Regulation number
876.5980
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
14Fr Colon Decompression Set, Macon Colon Decompression Set (K171619)Cook Ireland, Ltd.2017-08-01
MEDLINE ANTI-REFLUX VALVE (K132314)Medline Industries, Inc.2013-09-18
GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR (K053410)Kendall2006-01-06
NEXT GENERATION SALEM SUMP (K040388)Kendall2004-05-17
KNOTT NG TUBE (K971354)Michael M. Knott, M.D.1997-11-19
DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER (K960176)C.R. Bard, Inc.1996-07-24
ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBE (K926073)Surgimark, Inc.1995-05-15
ARGYLE SALEM SUMP TUBE ANTI-REFLUX VALVE INSERTION TRAY (K935781)Sherwood Medical Co.1995-01-27
LOPEZ VALVE WITH NG SUMP TUBE (K921104)Icu Medical, Inc.1992-10-26
WILSON-COOK COLON DECOMPRESSION SET (K900035)Wilson-Cook Medical, Inc.1990-03-07
KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE (K880850)Kmb Medical Products Co.1988-05-26
CATHETERS, DRAINAGE (K771048)Axiom Medical, Inc.1977-07-19

Recalls involving this device

No recalls on record reference this clearance.