97-TD Emerson Timer/Dimmer Control
FDA 510(k) K872937 · J. H. Emerson Co.
510(k) numberK872937
Submission
- Device name
- 97-TD Emerson Timer/Dimmer Control
- Applicant
- J. H. Emerson Co.
Cambridge, MA, US - Received
- July 27, 1987
- Decision date
- September 24, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- IQA – System, Environmental Control, Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.3725
- Specialty
- Physical Medicine
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More from Zofcom, Inc.
| 510(k) | Device | Decision |
|---|---|---|
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| K920910 | Oxygen Powered Resuscitator for CPRBTL · Traditional | 01/12/1993SE |
| K924174 | Emerson In-Exsufflator, Models 2-CM & 2-CANHJ · Traditional | 11/17/1992SE |
| K902764 | Emerson 33-AN Negative Pressure Respirator AlarmBYT · Traditional | 11/19/1990SE |
| K896721 | Model 7-AT Treatment ChamberLGM · Traditional | 01/22/1990SE |
| K881808 | Emerson Chest Respirator, Model 33-CREBYT · Traditional | 08/04/1988SE |
| K873489 | Emerson Dispos Thoracic Drainage Set - 551-8000GCX · Traditional | 12/29/1987SE |
| K872936 | 97-D Emerson Dimmer ControlIQA · Traditional | 09/24/1987SE |
| K864379 | Emerson 3MV Volume VentilatorCBK · Traditional | 12/15/1986SE |
| K864394 | Emerson 3MV Volume Ventilator · Traditional | 12/05/1986SE |
Questions and answers
When was 97-TD Emerson Timer/Dimmer Control cleared by the FDA?
97-TD Emerson Timer/Dimmer Control (K872937) received a 510(k) decision of Substantially Equivalent on September 24, 1987, 59 days after the submission was received.
What is the product code of K872937?
The FDA product code is IQA – System, Environmental Control, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.3725.