Medical Device Manufacturer · US , Mchenry , IL

Ritter Co. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1976

Total

Cleared

Denied

Ritter Co. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1976 to 1983. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Ritter Co. Filter by specialty or product code using the sidebar.

Ritter Co. 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 - Ritter Co.

10 devices

1-10 of 10

Cleared Oct 19, 1983

TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO

K831245 · DXN

Cardiovascular · 184d

Cleared Oct 04, 1983

SELF CHECK DIGITAL BLOOD PRESS. MONITOR

RITTER MODEL J DENTAL CHAIR

K800084 · KLC

Dental · 15d

Cleared Jul 17, 1978

ELECTROSURGICAL UNIT 75

K781101 · GEI

General & Plastic Surgery · 14d

Cleared Mar 14, 1978

ELECTROSURGICAL UNIT

K780293 · HAM

General & Plastic Surgery · 21d

Cleared Jan 03, 1978

DENTAL CHAIR, VANGUARD

RITTER STARLIGHT DENTAL OPERATING LIGHT

K760707 · EAZ

Dental · 12d

Ritter Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ritter Co.

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