Isotec Dispos. Pressure Transducer
FDA 510(k) K833884 · Delta Medical Industries
510(k) numberK833884
Submission
- Device name
- Isotec Dispos. Pressure Transducer
- Applicant
- Delta Medical Industries
Walker, MI, US - Received
- November 9, 1983
- Decision date
- April 17, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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| K820482 | Accu-Rynge Insulin Pump #SP-250FRN · Traditional | 03/26/1982SE |
| K810068 | Pediatric Arterial Blood FilterDTM · Traditional | 01/22/1981SE |
| K802755 | Arterial Blood Filter BF-37DTM · Traditional | 01/07/1981SE |
| K803102 | Arterial Bubble Trap K-20KRL · Traditional | 12/22/1980SE |
Questions and answers
When was Isotec Dispos. Pressure Transducer cleared by the FDA?
Isotec Dispos. Pressure Transducer (K833884) received a 510(k) decision of Substantially Equivalent on April 17, 1984, 160 days after the submission was received.