Riptide™ MAC-1200
by Micro Therapeutics, Inc. 3 variants
Riptide™ MAC-1200 is a Class II device made by Micro Therapeutics, Inc., cleared under FDA 510(k) K172448 on 21 Dec 2017 and listed in FDA GUDID since 16 Jul 2018 (UDI-DI 00847536029095), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00847536029095 | Date16 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172448 | Date21 Dec 2017 | StatusActive |
Official records
- AccessGUDID record 00847536029095
- FDA 510(k) database K172448
Across registries
- FDA 510(k) K172448 decided 21 Dec 2017 Active
- FDA GUDID UDI-DI 00847536029095 listed 16 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K172448
- Listed FDA GUDID 00847536029095
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Riptide™
- Generic name
- Surgical suction system collection container, single-use
- Model / reference
- MAC-1200
- Primary DI / UDI-DI
- 00847536029095
- 510(k) Number
- FDA product code
- NRY
- GMDN term
- Surgical suction system collection container, single-use
- Device class
- Class II
- Regulation number
- 870.1250
- GUDID distribution status
- In Commercial Distribution
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