Medical Device Manufacturer · US , Mchenry , IL

Robert Bosch Corp. - FDA 510(k) Cleared Devices

21 submissions · 18 cleared · Since 1979

Total

Cleared

Denied

Robert Bosch Corp. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1979 to 1986.

Browse the FDA 510(k) cleared devices submitted by Robert Bosch Corp. Filter by specialty or product code using the sidebar.

Robert Bosch Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Robert Bosch Corp.

21 devices

1-12 of 21

Cleared Jun 16, 1986

ERG 550 ERGOMETER BICYCLE

K854491 · DRT

Cardiovascular · 216d

Cleared Jun 16, 1986

ERG 551 ERGOMETER, BICYCLE

K854492 · DRT

Cardiovascular · 216d

Cleared Jun 16, 1986

ERG 555 COUCH ERGOMETER

K854493 · DRT

Cardiovascular · 216d

Cleared Mar 28, 1986

HV-4

K853154 · IPF

Physical Medicine · 242d

Cleared Mar 28, 1986

SP 4

K853541

Physical Medicine · 214d

Cleared Jan 16, 1986

HEARING AID ANALYSIS SYSTEM

K853271 · ETW

Ear, Nose, Throat · 164d

Cleared Aug 29, 1985

DEFI 502

K851485 · LDD

Cardiovascular · 136d

Cleared Aug 19, 1985

ECS 502

K840717 · DRT

Cardiovascular · 549d

Cleared Jul 17, 1985

SONOMED 4

K851937 · IMI

Physical Medicine · 93d

Cleared Apr 09, 1985

BOSCH IN THE EAR HEARING AID SUPERSTAR

K850188 · ESD

Ear, Nose, Throat · 81d

Cleared Mar 27, 1985

POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &

K850186

Gastroenterology & Urology · 68d

Cleared Mar 25, 1985

BODY HEARING AIDS MT 80 SP

K850185 · ESD

Ear, Nose, Throat · 66d

Robert Bosch Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Robert Bosch Corp.

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