Biosound Esaote, Inc.
Biosound Esaote, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2003, with 1 FDA device recall on record.
Top product codes for Biosound Esaote, Inc.
FDA recalls by Biosound Esaote, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Biosound Esaote, Inc.
- K023255 — TECHNOS MP, MODEL AU6
- K014168 — AU6 (TECHNOS/TECHNOS MP) ULTRASOUND IMAGING SYSTEM (ADDITION OF 3D IMAGING MODE AND MUSCULOSKELETAL INDICATION)
- K020164 — E-SCAN XQ
- K012728 — E-SCAN MRI SYSTEM
- K010405 — 7230 ULTRASOUND IMAGING SYSTEM WITH TEI
- K010057 — MODIFICATION TO ARTOSCAN M
- K001894 — MODIFICATION TO E-SCAN
- K000931 — AU5 ULTRASOUND IMAGING SYSTEM
- K000681 — AU5, AU6
- K994369 — 7250 (MEGAS)
- K990968 — E-SCAN
- K990360 — AU6
- K982444 — 7250 ULTRASOUND IMAGING SYSTEM
- K980468 — AU5 ULTRASOUND IMAGING SYSTEM
- K981358 — ARTOSCAN S
- K981293 — 7200 ULTRASOUND IMAGING SYSTEM
- K973922 — ARCHIMED 4210 AND 4220
- K974079 — FORMULA FOR ARCHIMED
- K971942 — SLED, FINGER, HANDLE
- K970703 — GALILEO HALLEY
Data sourced from openFDA. This site is unofficial and independent of the FDA.