Carrier, Amalgam, Operative

Device Code: 1221

Product Code(s): EKI

Device Classification Information

• Device Type ID: 1221
• Device Name: Carrier, Amalgam, Operative
• Regulation Description: Dental Hand Instrument.
• Regulation Medical Specialty: Dental
• Review Panel: Dental
• Premarket Review: Office Of Device Evaluation (ODE); Division Of Anesthesiology, General Hospital, Infection Control, And Dental Devices (DAGRID); Dental Devices Branch (DEDB)
• Submission Type: 510(K) Exempt
• CFR Regulation Number: 872.4565 [🔎]
• FDA Device Classification: Class 1 Medical Device
• Product Code: EKI
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

Recognized Standards

• 8-150 ISO 5832-9 Second Edition 2007-06-15
  Implants For Surgery - Metallic Materials - Part 9: Wrought High Nitrogen Stainless Steel
• 8-435 ISO 5832-1 Fifth Edition 2016-07-15
  Implants For Surgery - Metallic Materials - Part 1: Wrought Stainless Steel

Total Product Life Cycle

• Device Type ID: 1221
• Device: Carrier, Amalgam, Operative
• Product Code: EKI
• FDA Device Classification: Class 1 Medical Device
• Regulation Description: Dental Hand Instrument.
• CFR Regulation Number: 872.4565 [🔎]

Device Problems
Break	1
Total Device Problems	1

TPLC Last Update: 2019-04-02 19:50:13