UROMED PATCH
FDA 510(k) clearance K974600 · decided 1998-03-31
Clearance details
- K-number
- K974600
- Device name
- UROMED PATCH
- Applicant
- Uromed Corp.
- Decision
- Substantially Equivalent
- Date received
- 1997-12-09
- Decision date
- 1998-03-31
- Days to decision
- 112 days
- Clearance type
- Traditional
- Product code
- MNG
- Device class
- 1
- Regulation number
- 876.5160
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Needham, MA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| ORTHO CONTROL FEMALE URINARY CONTROL DEVICE (K010365) | Personal Products Co. | 2001-04-30 |
| RESTORE (AKA RE/STOR) (K983164) | Nebl, Inc. | 1999-03-05 |
| FEMASSIST FLEXIBLE (K974645) | Insight Medical Corp. | 1998-02-12 |
| RESTORE (A.K.A. CAPSURE) (K971359) | Nebl, Inc. | 1997-11-14 |
| FEMASSIST URINARY DEVICE (K963858) | Insight Medical Corp. | 1997-10-21 |
| MINIGUARD (K954215) | Advanced Surgical Intervention, Inc. | 1996-05-08 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| RELIANCE URINARY CONTROL INSERT & SIZING DEVICE (P960020/S001) | Uromed Corp. | 1999-04-01 |
| RELIANCE URINARY CONTROL INSERT AND SIZING DEVICE (P960020) | Uromed Corp. | 1996-08-16 |