Container System
FDA 510(k) K831068 · Adler Instrument Co.
510(k) numberK831068
Submission
- Device name
- Container System
- Applicant
- Adler Instrument Co.
Mchenry, IL, US - Received
- April 4, 1983
- Decision date
- May 9, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Adler Instrument Co.
| 510(k) | Device | Decision |
|---|---|---|
| K910171 | Maxi-Flow Suction Set W/Y ConnectorGAZ · Traditional | 02/01/1991SE |
| K910170 | Maxi-Flow Suction Set 12 Ft.GAZ · Traditional | 02/01/1991SE |
| K903209 | Maxi-Flow Insufflator Tubing Set W/FilterHES · Traditional | 12/21/1990SE |
| K903208 | Maxi-Flow Insufflator Tubing SetHES · Traditional | 12/17/1990SE |
| K900913 | Adler Disposable Bipolar CordHQO · Traditional | 04/04/1990SE |
| K841723 | Adler Custom Procedure Packs · Traditional | 08/01/1984SE |
| K833264 | Adler Steam Indicator-Gas IndicatorJOJ · Traditional | 11/03/1983SE |
Questions and answers
When was Container System cleared by the FDA?
Container System (K831068) received a 510(k) decision of Substantially Equivalent on May 9, 1983, 35 days after the submission was received.