Nd:Yag Laser Pulmonary Obstruction
FDA 510(k) K844458 · Endo Lase, Inc.
510(k) numberK844458
Submission
- Device name
- Nd:Yag Laser Pulmonary Obstruction
- Applicant
- Endo Lase, Inc.
Washington, DC, US - Received
- November 15, 1984
- Decision date
- January 3, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Endo Lase, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K853900 | Endo-Lase CD40 for NeurosurgeryGEX · Traditional | 06/18/1986SE |
| K853878 | Endo-Lase CD-100 CO2 Laser for NeurosurgeryGEX · Traditional | 05/02/1986SE |
| K855093 | Medilas 2 Nd:Yag Laser Surgery SystemHHR · Traditional | 02/21/1986SE |
| K853903 | Endo-Lase CD40 CO2 for GynecologyHHR · Traditional | 02/21/1986SE |
| K853876 | Endo-Lse CD-100 CO2 Laser for GynecologyHHR · Traditional | 02/21/1986SE |
| K853901 | Endo-Lase CD 40 for DermatologyGEX · Traditional | 02/19/1986SE |
| K853877 | Endo-Lase CD-100 CO2 Laser for DermatologyGEX · Traditional | 02/19/1986SE |
| K853580 | Medilas 2LKW · Traditional | 02/13/1986SE |
| K860152 | Model 700 Evacuator for Use with Laser SurgeryLNK · Traditional | 02/05/1986SE |
| K853902 | Endo-Lase CD40 for OtorhinolaryngologyEWG · Traditional | 01/09/1986SE |
Questions and answers
When was Nd:Yag Laser Pulmonary Obstruction cleared by the FDA?
Nd:Yag Laser Pulmonary Obstruction (K844458) received a 510(k) decision of Substantially Equivalent on January 3, 1985, 49 days after the submission was received.