Myelogram Procedure Tray
FDA 510(k) K852501 · Manan Manufacturing Co., Inc.
510(k) numberK852501
Submission
- Device name
- Myelogram Procedure Tray
- Applicant
- Manan Manufacturing Co., Inc.
Skokie, IL, US - Received
- June 12, 1985
- Decision date
- July 11, 1985
- Decision
- Unknown (SESD)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Manan Manufacturing Co., Inc.
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|---|---|---|
| K873208 | Manan Turner Style NeedleKNW · Traditional | 08/25/1987SE |
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| K863848 | Manan Brest Tumor Localization NeedleGAA · Traditional | 10/14/1986SE |
| K852018 | Arthrogram Tray for Double & Single Contrast Arthr · Traditional | 07/11/1985SESD |
| K851834 | Manan Gwi Guide Wire IntroducerDWS · Traditional | 07/11/1985SE |
| K851833 | Manan Seldinger NeedleDWS · Traditional | 07/11/1985SE |
| K851832 | Naman Potts Cournand NeedleDWS · Traditional | 07/11/1985SE |
| K852428 | Manan Epidural NeedleGCB · Traditional | 06/27/1985SE |
| K852427 | Manan Spinal NeedleGAA · Traditional | 06/27/1985SE |
| K852426 | Manan Trocar Style Biopsy NeedleGAA · Traditional | 06/27/1985SE |
Questions and answers
When was Myelogram Procedure Tray cleared by the FDA?
Myelogram Procedure Tray (K852501) received a 510(k) decision of Unknown on July 11, 1985, 29 days after the submission was received.