FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INCARE INTERMITTENT CATHETER
K Number: K013345
·
Decision Jan 7, 2002
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
85
Review Days
90
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Basic Information
- Device Name
- INCARE INTERMITTENT CATHETER
- K Number
- K013345
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5130
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Hollister, Inc.
- Date Received
- October 9, 2001
- Decision Date
- January 7, 2002
- Product Code
- KOD
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| KOD | Catheter, Urological | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Hollister, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K123804 | INSTAFLO BOWEL CATHETER SYSTEM KIT | Apr 17, 2013 | Substantially Equivalent |
| K100273 | INSTAFLO BOWEL CATHETER SYSTEM KIT | Apr 22, 2010 | Unknown |
| K090960 | VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184, | Aug 20, 2009 | Substantially Equivalent |
| K083153 | ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007 | Feb 4, 2009 | Unknown |
| K050483 | EVADRI BLADDER CONTROL SYSTEMS | Apr 12, 2005 | Substantially Equivalent |
| K040779 | RESTORE WOUND CLEANSER | May 17, 2004 | Substantially Equivalent |
| K013612 | INCARE PELVIC FLOOR THERAPY SYSTEM | Mar 19, 2002 | Substantially Equivalent |
| K013653 | INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE | Mar 5, 2002 | Substantially Equivalent |
| K013483 | INCARE ADVANCE; INTERMITTENT CATHETER, PLUS INTERMITTENT CATHETER, PLUS KIT | Jan 14, 2002 | Substantially Equivalent |
| K013141 | MICROGYN PLUS STIMULATION DEVICE | Dec 19, 2001 | Substantially Equivalent |