MDT Dental Chair
FDA 510(k) K931169 · Mdt Corp., Inc.
510(k) numberK931169
Submission
- Device name
- MDT Dental Chair
- Applicant
- Mdt Corp., Inc.
Rochester, NY, US - Received
- March 8, 1993
- Decision date
- May 20, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K942870 | Ultima 2 Dental ChairKLC · Traditional | Dentech Corp. | 02/27/1995SE |
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More from Planmeca USA, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K960777 | MDT Unispore and Spor-Test BiologicalindicatorFRC · Traditional | 05/23/1996SE |
| K942485 | MDT Urology TableMMZ · Traditional | 08/26/1994SE |
| K942486 | Image Full Power Examination/Minor Surgery TableFQO · Traditional | 08/10/1994SE |
| K924380 | Mdt/Harvey Model 7000 & 8000 ChemiclaveMLR · Traditional | 02/16/1994SE |
| K926081 | Dental LightEAZ · Traditional | 01/26/1994SE |
| K924955 | Mdt/Harvey MC-8 and MC-10FLE · Traditional | 10/15/1993SE |
| K932094 | Bovie Ultrasonic Surgical AspiratorLFL · Traditional | 07/21/1993SE |
| K920930 | Mdt/Castle 10/90 Dual Load StationFLF · Traditional | 03/31/1993SE |
| K922212 | MDT Castle Biosign Test PackFRC · Traditional | 08/10/1992SE |
| K914758 | Mdt/Shampaine Model 4900B Surgical TableGDC · Traditional | 12/19/1991SE |
Questions and answers
When was MDT Dental Chair cleared by the FDA?
MDT Dental Chair (K931169) received a 510(k) decision of Substantially Equivalent on May 20, 1993, 73 days after the submission was received.
What is the product code of K931169?
The FDA product code is KLC – Chair, Dental, With Operative Unit, a Class I (low risk) device regulated under 21 CFR 872.6250.