FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Medline Poly-Cath Red Polymer Urethral Catheter
K Number: K183335
·
Decision Jun 12, 2019
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
238
Review Days
191
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Basic Information
- Device Name
- Medline Poly-Cath Red Polymer Urethral Catheter
- K Number
- K183335
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5130
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medline Industries, Inc.
- Date Received
- December 3, 2018
- Decision Date
- June 12, 2019
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| GBM | Catheter, Urethral | FDA class 2 | Gastroenterology, Urology |
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