Drain, Tee (water Trap)

Device Code: 50

Product Code(s): BYH

Device Classification Information

• Device Type ID: 50
• Device Name: Drain, Tee (water Trap)
• Regulation Description: Tee Drain (water Trap).
• Regulation Medical Specialty: Anesthesiology
• Review Panel: Anesthesiology
• Premarket Review: Office Of Device Evaluation (ODE); Division Of Anesthesiology, General Hospital, Infection Control, And Dental Devices (DAGRID); Respiratory Devices Branch (RPDB)
• Submission Type: 510(K) Exempt
• CFR Regulation Number: 868.5995 [🔎]
• FDA Device Classification: Class 1 Medical Device
• Product Code: BYH
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

• Device Type ID: 50
• Device: Drain, Tee (water Trap)
• Product Code: BYH
• FDA Device Classification: Class 1 Medical Device
• Regulation Description: Tee Drain (water Trap).
• CFR Regulation Number: 868.5995 [🔎]

Device Problems
Leak / Splash	13
Total Device Problems	13

TPLC Last Update: 2019-04-02 19:27:26