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

VAPRO PLUS POCKET Intermittent Catheter

K Number: K152268 · Decision Sep 9, 2015
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
15
Review Days
29

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Basic Information

Device Name
VAPRO PLUS POCKET Intermittent Catheter
K Number
K152268
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hollister Incorporated
Date Received
August 11, 2015
Decision Date
September 9, 2015
Product Code
GBM
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
GBM Catheter, Urethral

Similar 510(k) Clearances

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

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Other Clearances by Hollister Incorporated

K Number Device Name
K253295 Coude Sleeved IC; Coude Plus Sleeved IC
K251468 Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket (name not finalized) Sleeved IC 3 Plus (name not finalized) Sleeved IC 3 Plus Pocket (name not finalized) (N/A)
K233524 Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus (Name not Finalized); Sleeved IC 2 Pocket (Name not Finalized); Sleeved IC 2 Plus Pocket (Name not Finalized)
K220667 Sleeved IC
K213575 Female IC (Not Finalized)
K211436 Intermittent Catheter (Not Finalized)
K193148 VaPro Plus Pocket, VaPro Plus
K191633 Infyna Chic
K183253 ValPro 2 Plus, VaPro 2 Plus Pocket
K180824 VaPro 2 Intermittent Catheter
Search all 15 clearances from Hollister Incorporated →