FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LAKE GASTROSTOMY TUBE

K Number: K902121 · Decision Jul 27, 1990
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
25
Applicant Total
15
Review Days
77

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Basic Information

Device Name
LAKE GASTROSTOMY TUBE
K Number
K902121
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Lake Medical Products, Inc.
Date Received
May 11, 1990
Decision Date
July 27, 1990
Product Code
KGC
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KGC Tube, Gastro-Enterostomy

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Other Clearances by Lake Medical Products, Inc.

K Number Device Name
K943162 LAKE STAGEZERO(TM) AIR FLOTATION BED
K922730 LAKE OSTOMY CARE SET
K905053 STAGE ZERO AIR FLOTATION BED
K901835 LAKE N/G FEEDING TUBE (WITH Y PORT CONNECTOR)
K902508 LAKE MALE EXTERNAL CATHETERIZATION KIT
K884127 LAKE N/G FEEDING TUBE
K884128 LAKE N/G EXTENSION SET
K883610 LAKE FOLEY CATHETERIZATION TRAY
K880578 LAKE DISPOSABLE PROBE COVER
K875383 LAKE CATHETER CARE KITS (MODIFICATION)
Search all 15 clearances from Lake Medical Products, Inc. →