ClearanceBrief
Company ยท US

Ritter Co.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1983. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXNSystem, Measurement, Blood-Pressure, Non-Invasive2
KLCChair, Dental, With Operative Unit2
EAYLight, Fiber Optic, Dental1
EAZLight, Operating, Dental1
EFBHandpiece, Air-Powered, Dental1
EIAUnit, Operative Dental1
GEIElectrosurgical, Cutting & Coagulation & Accessories1
HAMApparatus, Electrosurgical1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 19, 1983K831245TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO
Ritter Co.
DXN
Oct 4, 1983K832171SELF CHECK DIGITAL BLOOD PRESS. MONITOR
Ritter Co.
DXN
Aug 12, 1983K831976POWER OPTIC
Ritter Co.
EAY
Nov 22, 1982K823180SA-21 DENTAL UNIT
Ritter Co.
EIA
Jan 29, 1980K800084RITTER MODEL J DENTAL CHAIR
Ritter Co.
KLC
Jul 17, 1978K781101ELECTROSURGICAL UNIT 75
Ritter Co.
GEI
Mar 14, 1978K780293ELECTROSURGICAL UNIT
Ritter Co.
HAM
Jan 3, 1978K772300DENTAL CHAIR, VANGUARD
Ritter Co.
KLC
Nov 19, 1976K760929ACCUTORQ II
Ritter Co.
EFB
Oct 5, 1976K760707RITTER STARLIGHT DENTAL OPERATING LIGHT
Ritter Co.
EAZ

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes