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510(k) K800084

RITTER MODEL J DENTAL CHAIR by Ritter Co. — Product Code KLC

K800084 is an FDA 510(k) premarket notification submitted by Ritter Co. for the device "RITTER MODEL J DENTAL CHAIR". The FDA issued a decision of Substantially Equivalent on January 29, 1980. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. Ritter Co. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 29, 1980
Date Received
January 14, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Dental, With Operative Unit
Device Class
Class I
Regulation Number
872.6250
Review Panel
DE
Submission Type

Other clearances by Ritter Co.

  • K831245 — TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANO (October 19, 1983)
  • K832171 — SELF CHECK DIGITAL BLOOD PRESS. MONITOR (October 4, 1983)
  • K831976 — POWER OPTIC (August 12, 1983)
  • K823180 — SA-21 DENTAL UNIT (November 22, 1982)
  • K781101 — ELECTROSURGICAL UNIT 75 (July 17, 1978)
  • K780293 — ELECTROSURGICAL UNIT (March 14, 1978)
  • K772300 — DENTAL CHAIR, VANGUARD (January 3, 1978)
  • K760929 — ACCUTORQ II (November 19, 1976)
  • K760707 — RITTER STARLIGHT DENTAL OPERATING LIGHT (October 5, 1976)

Other clearances for product code KLC

  • K233921 — Luvis Chair (LC700C) (September 6, 2024)
  • K151987 — DCI Edge Dental Chair with Operative Unit (June 1, 2016)
  • K071353 — FOSHION CHAIR MOUNTED DENTAL, MODEL FJ48C (December 14, 2007)
  • K971063 — OPTIMA PLUS E DENTAL CHAIR; A DENTAL CHAIR; EXCEL CHAIR (June 3, 1997)
  • K963209 — PROSTYLE COMPACT (October 24, 1996)
  • K942870 — ULTIMA 2 DENTAL CHAIR (February 27, 1995)
  • K940950 — KAVO SYSTEMATICA 1060 (December 29, 1994)
  • K925567 — E 4000 DENTAL OPERATING CHAIR (March 10, 1994)
  • K923534 — PM2002 PROLINE (January 31, 1994)
  • K925119 — A-DEC 1040 CHAIR (January 31, 1994)

FDA data resources