Megadyne 1300U
by Megadyne Medical Products, Inc.
Megadyne 1300U is a Class II device made by Megadyne Medical Products, Inc., cleared under FDA 510(k) K050579 on 24 Mar 2005 and listed in FDA GUDID since 4 Sep 2018 (UDI-DI 10614559105290), active as of 23 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10614559105290 | Date4 Sep 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK050579 | Date24 Mar 2005 | StatusActive |
Official records
- AccessGUDID record 10614559105290
- FDA 510(k) database K050579
Across registries
- FDA 510(k) K050579 decided 24 Mar 2005 Active
- FDA GUDID UDI-DI 10614559105290 listed 4 Sep 2018 Listed
Recalls
-
- Terminated Z-2792-2018
If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the patient.
Timeline
- Cleared FDA 510(k) K050579
- Recall initiated FDA recalls Z-2792-2018
- Listed FDA GUDID 10614559105290
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Megadyne
- Generic name
- Electromechanical device/system transport trolley
- Model / Ref / Catalog
- 1300U
- Primary DI / UDI-DI
- 10614559105290
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Electromechanical device/system transport trolley
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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