ST-200A W/Maximal Voluntary Ventillat-
FDA 510(k) K843700 · Future Impex Corp.
510(k) numberK843700
Submission
- Device name
- ST-200A W/Maximal Voluntary Ventillat-
- Applicant
- Future Impex Corp.
Deerpark, NY, US - Received
- September 20, 1984
- Decision date
- October 24, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Future Impex Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K861487 | ST-90 Spiro AnalizerBTY · Traditional | 06/23/1986SE |
| K854687 | Erma Hb-Meter Model 303NKHG · Traditional | 06/04/1986SE |
| K854686 | TE-25 Coaguro MeterJBP · Traditional | 06/04/1986SE |
| K854685 | DIGITAL-9 Key Leucocyte CounterGKM · Traditional | 04/04/1986SE |
| K854678 | Erma PC-602 PC-603 Blood Cell CounterGKL · Traditional | 02/24/1986SE |
| K854677 | Erma PC-604 Blood Cell CounterGKL · Traditional | 02/24/1986SE |
| K854679 | PHOTIC-100 SpectrophotometerJJQ · Traditional | 02/20/1986SE |
| K843934 | Model {M-102 I-Channel Electro Cardiograph UnitDPS · Traditional | 11/20/1984SE |
| K843984 | PM-80 PulmotesterBZG · Traditional | 10/24/1984SE |
| K832433 | Automatic Spirometer ST-200BZG · Traditional | 09/29/1983SE |
Questions and answers
When was ST-200A W/Maximal Voluntary Ventillat- cleared by the FDA?
ST-200A W/Maximal Voluntary Ventillat- (K843700) received a 510(k) decision of Substantially Equivalent on October 24, 1984, 34 days after the submission was received.