Robert Bosch Corp.
Robert Bosch Corp. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1986.
Top product codes for Robert Bosch Corp.
Recent clearances by Robert Bosch Corp.
- K854491 — ERG 550 ERGOMETER BICYCLE
- K854492 — ERG 551 ERGOMETER, BICYCLE
- K854493 — ERG 555 COUCH ERGOMETER
- K853154 — HV-4
- K853541 — SP 4
- K853271 — HEARING AID ANALYSIS SYSTEM
- K851485 — DEFI 502
- K840717 — ECS 502
- K851937 — SONOMED 4
- K850188 — BOSCH IN THE EAR HEARING AID SUPERSTAR
- K850186 — POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &
- K850185 — BODY HEARING AIDS MT 80 SP
- K850187 — BOSCH STARR 66PP -HEARING AIDS
- K850189 — BOSCH STAR 66PP-S HEARING AID
- K850190 — STAR 66F-AGC-I HEARING AID
- K842803 — INTERFERENZ 4
- K842804 — DIADYN 4
- K842801 — ULTRAMED 11S601
- K842802 — VACOMED 4
- K842805 — IMPULS 3, IT SELECTOR
- K790682 — TONOTEST BLOOD PRESSURE DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.