MYA-1 and MYT-1 Myelogram Tray
FDA 510(k) K870418 · North Coast Medi-Tek
510(k) numberK870418
Submission
- Device name
- MYA-1 and MYT-1 Myelogram Tray
- Applicant
- North Coast Medi-Tek
Mentor, OH, US - Received
- February 3, 1987
- Decision date
- March 17, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from North Coast Medi-Tek
| 510(k) | Device | Decision |
|---|---|---|
| K870419 | Ivr-Sp Custom Angiography TrayDQO · Traditional | 05/11/1987SE |
| K870420 | PTC-6 and PTC-8 Percutaneous CholangiographyGBZ · Traditional | 04/14/1987SESD |
| K870416 | LP Extension SetsFPK · Traditional | 04/06/1987SE |
| K870417 | RCT-1, RCT-2, RCT-3 Arthrogram TrayFSM · Traditional | 03/05/1987SE |
| K854095 | Biopsy Tray I & IILRO · Traditional | 11/25/1985SESD |
Questions and answers
When was MYA-1 and MYT-1 Myelogram Tray cleared by the FDA?
MYA-1 and MYT-1 Myelogram Tray (K870418) received a 510(k) decision of Substantially Equivalent on March 17, 1987, 42 days after the submission was received.