Resubmittal of Mi 1000C Microimager
FDA 510(k) K881979 · Ausonics Pty , Ltd.
510(k) numberK881979
Submission
- Device name
- Resubmittal of Mi 1000C Microimager
- Applicant
- Ausonics Pty , Ltd.
Suffield, CT, US - Received
- May 12, 1988
- Decision date
- June 12, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JOP – Transducer, Ultrasonic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2880
- Specialty
- Cardiovascular
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| K933916 | Ausonics Opus 2 Realtime Ultrasound ScannerIYN · Traditional | 10/03/1994SE |
| K915715 | Cine Recall Function/Opus 1 Real Time ScannerIYO · Traditional | 07/02/1992SE |
| K920307 | Ausonics Opus 1 System, Annular Array OptionITX · Traditional | 05/19/1992SE |
| K905488 | Doppler Upgrade for Ausonics Opus 1 Real Time ScanLMB · Traditional | 12/18/1991SE |
| K902728 | 7.5 MHZ Bi Plane Rectal Probe (P/N: 041-815)ITX · Traditional | 02/13/1991SE |
| K896714 | Ausonics 5000IYO · Traditional | 06/11/1990SE |
| K884299 | Apa-C Catalog Number A-8001-CIYO · Traditional | 01/10/1989SE |
| K883925 | UroimagerIYO · Traditional | 12/15/1988SE |
| K883079 | WWDS-005 Human Rectal ProbeIYO · Traditional | 12/14/1988SE |
| K883372 | Alpha MC-9S Mobil C-Arm Image Intensifier UnitJAA · Traditional | 11/25/1988SE |
Questions and answers
When was Resubmittal of Mi 1000C Microimager cleared by the FDA?
Resubmittal of Mi 1000C Microimager (K881979) received a 510(k) decision of Substantially Equivalent on June 12, 1989, 396 days after the submission was received.
What is the product code of K881979?
The FDA product code is JOP – Transducer, Ultrasonic, a Class II (moderate risk) device regulated under 21 CFR 870.2880.