Dryden Scavenger Interface System
FDA 510(k) K842843 · Dryden Corp.
510(k) numberK842843
Submission
- Device name
- Dryden Scavenger Interface System
- Applicant
- Dryden Corp.
Mchenry, IL, US - Received
- July 20, 1984
- Decision date
- July 27, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Dryden Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K880923 | Patient Ventilator IsolatorCBK · Traditional | 09/06/1988SE |
| K880769 | Breathing Circuit W/Heated WireBZE · Traditional | 08/24/1988SE |
| K882285 | Nonrebreathing CircuitBTM · Traditional | 08/16/1988SE |
| K873928 | Universal TourniquetGAX · Traditional | 10/23/1987SE |
| K873927 | Reuseable Breathing TubesBZO · Traditional | 10/20/1987SE |
| K870859 | Bag-Tail Bleed ValveCAI · Traditional | 08/03/1987SE |
| K871386 | Breathing CircuitCAI · Traditional | 05/29/1987SE |
| K870858 | Badgwell Sampling CatheterCCK · Traditional | 05/14/1987SE |
| K861540 | Disposable Berman and Guedel AirwaysCAE · Traditional | 05/02/1986SE |
| K850644 | Nasopharyngeal Airway-RobertazziBTQ · Traditional | 03/21/1985SE |
Questions and answers
When was Dryden Scavenger Interface System cleared by the FDA?
Dryden Scavenger Interface System (K842843) received a 510(k) decision of Substantially Equivalent on July 27, 1984, 7 days after the submission was received.