FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

LAKE MALE EXTERNAL CATHETERIZATION KIT

K Number: K902508 · Decision Aug 23, 1990
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
59
Applicant Total
15
Review Days
79

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Basic Information

Device Name
LAKE MALE EXTERNAL CATHETERIZATION KIT
K Number
K902508
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Applicant
Lake Medical Products, Inc.
Date Received
June 5, 1990
Decision Date
August 23, 1990
Product Code
FCM
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
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)

Similar 510(k) Clearances

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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)
K902121 LAKE GASTROSTOMY TUBE
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. →