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

E-Z HOLD WITH ADHESIVE BASE.-#4065

K Number: K864188 · Decision Dec 4, 1986
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
5
Review Days
38

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Basic Information

Device Name
E-Z HOLD WITH ADHESIVE BASE.-#4065
K Number
K864188
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
John F. Greer Co., Inc.
Date Received
October 27, 1986
Decision Date
December 4, 1986
Product Code
KNX
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
KNX Collector, Urine, (And Accessories) For Indwelling Catheter

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNX), ordered by most recent decision date.

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Other Clearances by John F. Greer Co., Inc.

K Number Device Name
K870577 E-Z LOOP
K870531 EZ TAC FILTER
K864190 E-Z HOLD - #4060
K864189 ULTRA-GEL - #4083