Laser Mirror
FDA 510(k) K840982 · American V. Mueller
510(k) numberK840982
Submission
- Device name
- Laser Mirror
- Applicant
- American V. Mueller
Mchenry, IL, US - Received
- March 6, 1984
- Decision date
- March 6, 1984
- Decision
- Unknown (SESP)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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| K864676 | Heyer-Schulte Hermetic External CSF Drain. SystemJXG · Traditional | 12/29/1986SE |
| K862772 | V. Mueller (R) Gooseneck Circular StaplerGAG · Traditional | 08/18/1986SE |
| K861471 | V. Mueller Vital Clip-Hemostatic ClipFZP · Traditional | 06/06/1986SE |
| K854568 | V. Mueller Pneumo-Intestinal 15 Vascular & 30 StapGEF · Traditional | 12/02/1985SE |
| K854049 | Heyer-Schulte Syringo Peritoneal ShuntJXG · Traditional | 11/27/1985SE |
| K851082 | V. Mueller Blom-Singer Esophageal Insufflation TesENW · Traditional | 07/22/1985SE |
| K851974 | V. Mueller Vital Skin StaplerGDT · Traditional | 06/11/1985SE |
Questions and answers
When was Laser Mirror cleared by the FDA?
Laser Mirror (K840982) received a 510(k) decision of Unknown on March 6, 1984, 0 days after the submission was received.